rs7523622

Homo sapiens
C>A
LOC105378768 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0018 (545/29970,GnomAD)
A=0025 (754/29118,TOPMED)
A=0021 (105/5008,1000G)
chr1:62424839 (GRCh38.p7) (1p31.3)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.62424839C>A
GRCh37.p13 chr 1NC_000001.10:g.62890510C>A

Gene: LOC105378768, uncharacterized LOC105378768(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC105378768 transcriptXR_947449.2:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.926A=0.074
1000GenomesAmericanSub694C=0.990A=0.010
1000GenomesEast AsianSub1008C=1.000A=0.000
1000GenomesEuropeSub1006C=0.999A=0.001
1000GenomesGlobalStudy-wide5008C=0.979A=0.021
1000GenomesSouth AsianSub978C=1.000A=0.000
The Genome Aggregation DatabaseAfricanSub8726C=0.939A=0.061
The Genome Aggregation DatabaseAmericanSub838C=0.990A=0.010
The Genome Aggregation DatabaseEast AsianSub1618C=1.000A=0.000
The Genome Aggregation DatabaseEuropeSub18486C=0.999A=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29970C=0.981A=0.018
The Genome Aggregation DatabaseOtherSub302C=1.000A=0.000
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.974A=0.025
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs75236220.000862alcohol dependence21314694

eQTL of rs7523622 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 rs7523622 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 )
chr16292369462924069E06733184
chr16285007462850282E068-40228
chr16285034562850692E068-39818
chr16284977262849878E069-40632
chr16284992462850006E069-40504
chr16285007462850282E069-40228
chr16285034562850692E069-39818
chr16285034562850692E070-39818
chr16285166362852887E070-37623
chr16286523362865341E070-25169
chr16286652462866604E070-23906
chr16286665962867175E070-23335
chr16290575562905955E07015245
chr16284977262849878E071-40632
chr16284992462850006E071-40504
chr16285007462850282E071-40228
chr16285034562850692E071-39818
chr16285090662851015E071-39495
chr16286110062861424E071-29086
chr16286652462866604E071-23906
chr16286665962867175E071-23335
chr16290001262900248E0719502
chr16284977262849878E072-40632
chr16284992462850006E072-40504
chr16285007462850282E072-40228
chr16285034562850692E072-39818
chr16286110062861424E072-29086
chr16292369462924069E07233184
chr16285007462850282E073-40228
chr16285034562850692E073-39818
chr16285090662851015E073-39495
chr16284977262849878E074-40632
chr16284992462850006E074-40504
chr16285007462850282E074-40228
chr16285034562850692E074-39818
chr16285090662851015E074-39495
chr16285981262859872E074-30638
chr16286110062861424E074-29086








Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr16290096862904238E06710458
chr16290096862904238E06810458
chr16290096862904238E06910458
chr16290096862904238E07010458
chr16290096862904238E07110458
chr16290096862904238E07210458
chr16290096862904238E07310458
chr16290096862904238E07410458
chr16290096862904238E08110458
chr16290096862904238E08210458