rs10735366

Homo sapiens
G>A
ANKS1B : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0033 (1013/29968,GnomAD)
G==0023 (678/29118,TOPMED)
G==0017 (86/5008,1000G)
G==0042 (161/3854,ALSPAC)
G==0041 (153/3708,TWINSUK)
chr12:99372428 (GRCh38.p7) (12q23.1)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 12NC_000012.12:g.99372428G>A
GRCh37.p13 chr 12NC_000012.11:g.99766206G>A
ANKS1B RefSeqGeneNG_029860.1:g.617227C>T

Gene: ANKS1B, ankyrin repeat and sterile alpha motif domain containing 1B(minus strand)

Molecule type Change Amino acid[Codon] SO Term
ANKS1B transcript variant 1NM_152788.4:c.N/AIntron Variant
ANKS1B transcript variant 4NM_001204065.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 5NM_001204066.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 6NM_001204067.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 7NM_001204068.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 8NM_001204069.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 9NM_001204070.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 10NM_001204079.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 11NM_001204080.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 12NM_001204081.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 3NM_020140.3:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant 2NM_181670.3:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X9XM_005269028.4:c.N/AIntron Variant
ANKS1B transcript variant X13XM_005269029.4:c.N/AIntron Variant
ANKS1B transcript variant X2XM_006719504.3:c.N/AIntron Variant
ANKS1B transcript variant X3XM_006719505.3:c.N/AIntron Variant
ANKS1B transcript variant X4XM_006719506.3:c.N/AIntron Variant
ANKS1B transcript variant X6XM_006719507.3:c.N/AIntron Variant
ANKS1B transcript variant X10XM_006719508.3:c.N/AIntron Variant
ANKS1B transcript variant X11XM_006719509.3:c.N/AIntron Variant
ANKS1B transcript variant X16XM_006719510.3:c.N/AIntron Variant
ANKS1B transcript variant X18XM_006719512.3:c.N/AIntron Variant
ANKS1B transcript variant X19XM_006719513.3:c.N/AIntron Variant
ANKS1B transcript variant X21XM_006719514.3:c.N/AIntron Variant
ANKS1B transcript variant X14XM_011538571.2:c.N/AIntron Variant
ANKS1B transcript variant X1XM_017019651.1:c.N/AIntron Variant
ANKS1B transcript variant X5XM_017019652.1:c.N/AIntron Variant
ANKS1B transcript variant X7XM_017019653.1:c.N/AIntron Variant
ANKS1B transcript variant X8XM_017019654.1:c.N/AIntron Variant
ANKS1B transcript variant X12XM_017019655.1:c.N/AIntron Variant
ANKS1B transcript variant X15XM_017019656.1:c.N/AIntron Variant
ANKS1B transcript variant X17XM_017019657.1:c.N/AIntron Variant
ANKS1B transcript variant X20XM_017019658.1:c.N/AIntron Variant
ANKS1B transcript variant X30XM_005269032.3:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X23XM_017019659.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X24XM_017019660.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X25XM_017019661.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X26XM_017019662.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X27XM_017019663.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X28XM_017019664.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X29XM_017019665.1:c.N/AGenic Upstream Transcript Variant
ANKS1B transcript variant X22XR_001748815.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.001A=0.999
1000GenomesAmericanSub694G=0.020A=0.980
1000GenomesEast AsianSub1008G=0.001A=0.999
1000GenomesEuropeSub1006G=0.037A=0.963
1000GenomesGlobalStudy-wide5008G=0.017A=0.983
1000GenomesSouth AsianSub978G=0.030A=0.970
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.042A=0.958
The Genome Aggregation DatabaseAfricanSub8734G=0.008A=0.992
The Genome Aggregation DatabaseAmericanSub836G=0.020A=0.980
The Genome Aggregation DatabaseEast AsianSub1620G=0.001A=0.999
The Genome Aggregation DatabaseEuropeSub18476G=0.049A=0.950
The Genome Aggregation DatabaseGlobalStudy-wide29968G=0.033A=0.966
The Genome Aggregation DatabaseOtherSub302G=0.040A=0.960
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.023A=0.976
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.041A=0.959
PMID Title Author Journal
19268276Genome-wide association study of smoking initiation and current smoking.Vink JMAm J Hum Genet

P-Value

SNP ID p-value Traits Study
rs107353660.000846nicotine smoking19268276

eQTL of rs10735366 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs10735366 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr129972550199725607E070-40599
chr129972670199726828E070-39378
chr129972684699726947E070-39259
chr129972725199727390E070-38816
chr129972835099728400E070-37806
chr129972850699728868E070-37338
chr129978214799782655E07015941
chr129978268499782786E07016478
chr129978279399782941E07016587
chr129972616899726260E073-39946
chr129972670199726828E073-39378
chr129977962699779676E08213420
chr129977971399779840E08213507