rs9463046

Homo sapiens
T>C
SUPT3H : Intron Variant
LOC107986600 : Non Coding Transcript Variant
Check p-value
SNV (Single Nucleotide Variation)
C=0083 (2495/29942,GnomAD)
C=0107 (3117/29118,TOPMED)
C=0096 (482/5008,1000G)
C=0039 (152/3854,ALSPAC)
C=0030 (113/3708,TWINSUK)
chr6:44834981 (GRCh38.p7) (6p21.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.44834981T>C
GRCh37.p13 chr 6NC_000006.11:g.44802718T>C

Gene: SUPT3H, SPT3 homolog, SAGA and STAGA complex component(minus strand)

Molecule type Change Amino acid[Codon] SO Term
SUPT3H transcript variant 3NM_001261823.1:c.N/AIntron Variant
SUPT3H transcript variant 1NM_003599.3:c.N/AIntron Variant
SUPT3H transcript variant 2NM_181356.2:c.N/AIntron Variant
SUPT3H transcript variant X4XM_011514949.2:c.N/AIntron Variant
SUPT3H transcript variant X6XM_011514950.1:c.N/AIntron Variant
SUPT3H transcript variant X7XM_011514951.2:c.N/AIntron Variant
SUPT3H transcript variant X8XM_011514952.2:c.N/AIntron Variant
SUPT3H transcript variant X8XM_011514953.2:c.N/AIntron Variant
SUPT3H transcript variant X10XM_011514954.2:c.N/AIntron Variant
SUPT3H transcript variant X3XM_017011369.1:c.N/AIntron Variant
SUPT3H transcript variant X5XM_017011370.1:c.N/AIntron Variant
SUPT3H transcript variant X11XM_017011371.1:c.N/AIntron Variant
SUPT3H transcript variant X14XM_017011372.1:c.N/AIntron Variant
SUPT3H transcript variant X16XM_017011373.1:c.N/AIntron Variant
SUPT3H transcript variant X21XM_017011374.1:c.N/AIntron Variant
SUPT3H transcript variant X2XR_001743685.1:n.N/AIntron Variant
SUPT3H transcript variant X12XR_001743686.1:n.N/AIntron Variant
SUPT3H transcript variant X15XR_001743687.1:n.N/AIntron Variant
SUPT3H transcript variant X13XR_001743688.1:n.N/AIntron Variant
SUPT3H transcript variant X19XR_001743689.1:n.N/AIntron Variant
SUPT3H transcript variant X17XR_001743691.1:n.N/AIntron Variant
SUPT3H transcript variant X1XR_926319.2:n.N/AIntron Variant
SUPT3H transcript variant X20XR_001743690.1:n.N/AGenic Downstream Transcript Variant
SUPT3H transcript variant X18XR_001743692.1:n.N/AGenic Downstream Transcript Variant
SUPT3H transcript variant X10XR_926320.1:n.N/AGenic Downstream Transcript Variant
SUPT3H transcript variant X14XR_926321.1:n.N/AGenic Downstream Transcript Variant

Gene: LOC107986600, uncharacterized LOC107986600(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC107986600 transcriptXR_001744142.1:n....XR_001744142.1:n.3963T>CT>CNon Coding Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.754C=0.246
1000GenomesAmericanSub694T=0.920C=0.080
1000GenomesEast AsianSub1008T=0.996C=0.004
1000GenomesEuropeSub1006T=0.952C=0.048
1000GenomesGlobalStudy-wide5008T=0.904C=0.096
1000GenomesSouth AsianSub978T=0.950C=0.050
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.961C=0.039
The Genome Aggregation DatabaseAfricanSub8702T=0.810C=0.190
The Genome Aggregation DatabaseAmericanSub838T=0.890C=0.110
The Genome Aggregation DatabaseEast AsianSub1616T=0.999C=0.001
The Genome Aggregation DatabaseEuropeSub18484T=0.959C=0.040
The Genome Aggregation DatabaseGlobalStudy-wide29942T=0.916C=0.083
The Genome Aggregation DatabaseOtherSub302T=0.970C=0.030
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.893C=0.107
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.970C=0.030
PMID Title Author Journal
23953852Genome-wide association studies of maximum number of drinks.Pan YJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs94630461.62E-05alcohol consumption23953852

eQTL of rs9463046 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 rs9463046 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 )
chr64481030844811350E0697590
chr64482359644824311E07020878
chr64482436644824465E07021648
chr64482563944825910E07022921
chr64482592244826044E07023204
chr64482672744826785E07024009
chr64482686444827997E07024146
chr64476784744768497E071-34221
chr64482359644824311E07320878
chr64482436644824465E07321648
chr64481030844811350E0747590
chr64481161344811657E0748895
chr64481177444811883E0749056
chr64482359644824311E08120878
chr64482436644824465E08121648
chr64482436644824465E08221648
chr64482563944825910E08222921
chr64482592244826044E08223204
chr64482672744826785E08224009