rs7603576

Homo sapiens
A>G
LOC105373718 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0198 (5924/29922,GnomAD)
G=0197 (5757/29118,TOPMED)
G=0181 (907/5008,1000G)
G=0227 (876/3854,ALSPAC)
G=0221 (821/3708,TWINSUK)
chr2:160575093 (GRCh38.p7) (2q24.2)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.160575093A>G
GRCh37.p13 chr 2NC_000002.11:g.161431604A>G

Gene: LOC105373718, uncharacterized LOC105373718(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC105373718 transcriptXR_923526.2:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.875G=0.125
1000GenomesAmericanSub694A=0.610G=0.390
1000GenomesEast AsianSub1008A=0.978G=0.022
1000GenomesEuropeSub1006A=0.767G=0.233
1000GenomesGlobalStudy-wide5008A=0.819G=0.181
1000GenomesSouth AsianSub978A=0.780G=0.220
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.773G=0.227
The Genome Aggregation DatabaseAfricanSub8712A=0.847G=0.153
The Genome Aggregation DatabaseAmericanSub836A=0.620G=0.380
The Genome Aggregation DatabaseEast AsianSub1618A=0.975G=0.025
The Genome Aggregation DatabaseEuropeSub18456A=0.774G=0.225
The Genome Aggregation DatabaseGlobalStudy-wide29922A=0.802G=0.198
The Genome Aggregation DatabaseOtherSub300A=0.730G=0.270
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.802G=0.197
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.779G=0.221
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs76035760.0000465alcoholismpha002892
rs76035760.000047alcohol dependence20201924

eQTL of rs7603576 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 rs7603576 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.