rs770172

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0353 (10585/29938,GnomAD)
G=0350 (10190/29118,TOPMED)
G=0439 (2201/5008,1000G)
G=0338 (1304/3854,ALSPAC)
G=0331 (1227/3708,TWINSUK)
chr5:107785718 (GRCh38.p7) (5q21.3)
AD
GWASdb2
1   publication(s)
See rs on genome
6 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.107785718A>G
GRCh37.p13 chr 5NC_000005.9:g.107121419A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.607G=0.393
1000GenomesAmericanSub694A=0.560G=0.440
1000GenomesEast AsianSub1008A=0.377G=0.623
1000GenomesEuropeSub1006A=0.678G=0.322
1000GenomesGlobalStudy-wide5008A=0.561G=0.439
1000GenomesSouth AsianSub978A=0.560G=0.440
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.662G=0.338
The Genome Aggregation DatabaseAfricanSub8704A=0.608G=0.392
The Genome Aggregation DatabaseAmericanSub838A=0.560G=0.440
The Genome Aggregation DatabaseEast AsianSub1612A=0.370G=0.630
The Genome Aggregation DatabaseEuropeSub18482A=0.691G=0.308
The Genome Aggregation DatabaseGlobalStudy-wide29938A=0.646G=0.353
The Genome Aggregation DatabaseOtherSub302A=0.710G=0.290
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.650G=0.350
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.669G=0.331
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
rs7701726.52E-05alcohol withdrawal symptoms22072270

eQTL of rs770172 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 rs770172 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 )
chr5107140779107141147E07019360
chr5107141604107141709E07020185
chr5107142042107142355E07020623
chr5107144282107144943E07022863
chr5107170392107170499E08148973
chr5107170668107171289E08149249