rs6677435

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0052 (1579/29950,GnomAD)
A=0042 (1222/29118,TOPMED)
A=0100 (500/5008,1000G)
A=0040 (154/3854,ALSPAC)
A=0046 (169/3708,TWINSUK)
chr1:195821528 (GRCh38.p7) (1q31.3)
CD
GWASdb2 | GWASCatalog
1   publication(s)
See rs on genome
3 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.195821528G>A
GRCh37.p13 chr 1NC_000001.10:g.195790658G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.994A=0.006
1000GenomesAmericanSub694G=0.870A=0.130
1000GenomesEast AsianSub1008G=0.733A=0.267
1000GenomesEuropeSub1006G=0.958A=0.042
1000GenomesGlobalStudy-wide5008G=0.900A=0.100
1000GenomesSouth AsianSub978G=0.910A=0.090
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.960A=0.040
The Genome Aggregation DatabaseAfricanSub8718G=0.985A=0.015
The Genome Aggregation DatabaseAmericanSub836G=0.860A=0.140
The Genome Aggregation DatabaseEast AsianSub1614G=0.708A=0.292
The Genome Aggregation DatabaseEuropeSub18480G=0.954A=0.045
The Genome Aggregation DatabaseGlobalStudy-wide29950G=0.947A=0.052
The Genome Aggregation DatabaseOtherSub302G=0.950A=0.050
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.958A=0.042
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.954A=0.046
PMID Title Author Journal
23958962Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.Gelernter JMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs66774350.000009cocaine dependence23958962
rs66774359.00E-06cocaine dependence23958962

eQTL of rs6677435 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 rs6677435 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 )
chr1195835188195835756E07444530
chr1195835188195835756E08144530
chr1195750810195750918E082-39740