rs6677934

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0130 (3896/29968,GnomAD)
G=0161 (4701/29118,TOPMED)
G=0145 (724/5008,1000G)
G=0068 (263/3854,ALSPAC)
G=0073 (271/3708,TWINSUK)
chr1:206615113 (GRCh38.p7) (1q32.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.206615113A>G
GRCh37.p13 chr 1 fix patch HG1293_PATCHNW_003871057.1:g.605967A>G
GRCh37.p13 chr 1NC_000001.10:g.206788458A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.727G=0.273
1000GenomesAmericanSub694A=0.900G=0.100
1000GenomesEast AsianSub1008A=0.944G=0.056
1000GenomesEuropeSub1006A=0.926G=0.074
1000GenomesGlobalStudy-wide5008A=0.855G=0.145
1000GenomesSouth AsianSub978A=0.830G=0.170
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.932G=0.068
The Genome Aggregation DatabaseAfricanSub8722A=0.762G=0.238
The Genome Aggregation DatabaseAmericanSub838A=0.880G=0.120
The Genome Aggregation DatabaseEast AsianSub1618A=0.933G=0.067
The Genome Aggregation DatabaseEuropeSub18488A=0.914G=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29968A=0.870G=0.130
The Genome Aggregation DatabaseOtherSub302A=0.890G=0.110
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.838G=0.161
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.927G=0.073
PMID Title Author Journal
22072270Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms.Wang KSJ Neural Transm (Vienna)

P-Value

SNP ID p-value Traits Study
rs66779348.11E-05alcohol withdrawal symptoms22072270

eQTL of rs6677934 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 rs6677934 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.