rs17203601

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0161 (4836/29950,GnomAD)
A=0130 (3810/29118,TOPMED)
A=0129 (646/5008,1000G)
A=0217 (838/3854,ALSPAC)
A=0226 (837/3708,TWINSUK)
chr18:24577590 (GRCh38.p7) (18q11.2)
AD
GWASdb2
1   publication(s)
See rs on genome
7 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 18NC_000018.10:g.24577590G>A
GRCh37.p13 chr 18NC_000018.9:g.22157554G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.988A=0.012
1000GenomesAmericanSub694G=0.880A=0.120
1000GenomesEast AsianSub1008G=0.882A=0.118
1000GenomesEuropeSub1006G=0.763A=0.237
1000GenomesGlobalStudy-wide5008G=0.871A=0.129
1000GenomesSouth AsianSub978G=0.800A=0.200
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.783A=0.217
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.869A=0.130
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.774A=0.226
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
rs172036010.000165alcohol dependence21314694

eQTL of rs17203601 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 rs17203601 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 )
chr182217591522176113E06818361
chr182213940122139834E070-17720
chr182213999622140046E070-17508
chr182217591522176113E07118361
chr182212025322120484E073-37070
chr182212051422120594E073-36960
chr182212073922120779E073-36775