rs10224675

Homo sapiens
A>G
TPK1 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0026 (792/29862,GnomAD)
G=0036 (1065/29118,TOPMED)
G=0027 (137/5008,1000G)
G=0000 (1/3854,ALSPAC)
G=0001 (4/3708,TWINSUK)
chr7:144595669 (GRCh38.p7) (7q35)
AD
GWASdb2
2   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.144595669A>G
GRCh37.p13 chr 7NC_000007.13:g.144292762A>G
TPK1 RefSeqGeneNG_032112.1:g.245385T>C

Gene: TPK1, thiamin pyrophosphokinase 1(minus strand)

Molecule type Change Amino acid[Codon] SO Term
TPK1 transcript variant 2NM_001042482.1:c.N/AIntron Variant
TPK1 transcript variant 1NM_022445.3:c.N/AIntron Variant
TPK1 transcript variant X11XM_005249970.1:c.N/AIntron Variant
TPK1 transcript variant X1XM_011516031.1:c.N/AIntron Variant
TPK1 transcript variant X3XM_011516032.2:c.N/AIntron Variant
TPK1 transcript variant X2XM_011516033.2:c.N/AIntron Variant
TPK1 transcript variant X4XM_011516034.2:c.N/AIntron Variant
TPK1 transcript variant X7XM_011516035.2:c.N/AIntron Variant
TPK1 transcript variant X8XM_011516037.2:c.N/AIntron Variant
TPK1 transcript variant X13XM_011516039.2:c.N/AIntron Variant
TPK1 transcript variant X15XM_011516040.2:c.N/AIntron Variant
TPK1 transcript variant X21XM_011516041.2:c.N/AIntron Variant
TPK1 transcript variant X16XM_011516043.1:c.N/AIntron Variant
TPK1 transcript variant X25XM_011516044.1:c.N/AIntron Variant
TPK1 transcript variant X24XM_011516047.2:c.N/AIntron Variant
TPK1 transcript variant X23XM_011516048.1:c.N/AIntron Variant
TPK1 transcript variant X37XM_011516050.1:c.N/AIntron Variant
TPK1 transcript variant X5XM_017011969.1:c.N/AIntron Variant
TPK1 transcript variant X7XM_017011970.1:c.N/AIntron Variant
TPK1 transcript variant X9XM_017011971.1:c.N/AIntron Variant
TPK1 transcript variant X10XM_017011972.1:c.N/AIntron Variant
TPK1 transcript variant X12XM_017011973.1:c.N/AIntron Variant
TPK1 transcript variant X12XM_017011974.1:c.N/AIntron Variant
TPK1 transcript variant X14XM_017011975.1:c.N/AIntron Variant
TPK1 transcript variant X18XM_017011976.1:c.N/AIntron Variant
TPK1 transcript variant X19XM_017011977.1:c.N/AIntron Variant
TPK1 transcript variant X20XM_017011978.1:c.N/AIntron Variant
TPK1 transcript variant X24XM_017011979.1:c.N/AIntron Variant
TPK1 transcript variant X26XM_017011980.1:c.N/AIntron Variant
TPK1 transcript variant X27XM_017011981.1:c.N/AIntron Variant
TPK1 transcript variant X22XM_017011982.1:c.N/AIntron Variant
TPK1 transcript variant X30XM_017011983.1:c.N/AIntron Variant
TPK1 transcript variant X31XM_017011984.1:c.N/AIntron Variant
TPK1 transcript variant X34XM_017011985.1:c.N/AIntron Variant
TPK1 transcript variant X36XM_017011986.1:c.N/AIntron Variant
TPK1 transcript variant X21XM_011516046.1:c.N/AGenic Downstream Transcript Variant
TPK1 transcript variant X17XR_001744630.1:n.N/AIntron Variant
TPK1 transcript variant X6XR_927446.2:n.N/AIntron Variant
TPK1 transcript variant X35XR_927453.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.900G=0.100
1000GenomesAmericanSub694A=0.990G=0.010
1000GenomesEast AsianSub1008A=1.000G=0.000
1000GenomesEuropeSub1006A=0.999G=0.001
1000GenomesGlobalStudy-wide5008A=0.973G=0.027
1000GenomesSouth AsianSub978A=1.000G=0.000
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=1.000G=0.000
The Genome Aggregation DatabaseAfricanSub8706A=0.911G=0.089
The Genome Aggregation DatabaseAmericanSub836A=0.990G=0.010
The Genome Aggregation DatabaseEast AsianSub1620A=1.000G=0.000
The Genome Aggregation DatabaseEuropeSub18398A=0.999G=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29862A=0.973G=0.026
The Genome Aggregation DatabaseOtherSub302A=1.000G=0.000
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.963G=0.036
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.999G=0.001
PMID Title Author Journal
20202923A genome-wide association study of alcohol dependence.Bierut LJProc Natl Acad Sci U S A
21956439Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.Zuo LNeuropsychopharmacology

P-Value

SNP ID p-value Traits Study
rs102246753.8E-05alcohol dependence21956439

eQTL of rs10224675 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 rs10224675 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.