rs16986005

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0013 (402/29526,GnomAD)
A=0020 (598/29118,TOPMED)
A=0010 (48/5008,1000G)
chr20:41712483 (GRCh38.p7) (20q12)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 20NC_000020.11:g.41712483G>A
GRCh37.p13 chr 20NC_000020.10:g.40341122G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.964A=0.036
1000GenomesAmericanSub694G=1.000A=0.000
1000GenomesEast AsianSub1008G=1.000A=0.000
1000GenomesEuropeSub1006G=1.000A=0.000
1000GenomesGlobalStudy-wide5008G=0.990A=0.010
1000GenomesSouth AsianSub978G=1.000A=0.000
The Genome Aggregation DatabaseAfricanSub8644G=0.954A=0.046
The Genome Aggregation DatabaseAmericanSub838G=1.000A=0.000
The Genome Aggregation DatabaseEast AsianSub1620G=1.000A=0.000
The Genome Aggregation DatabaseEuropeSub18124G=0.999A=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29526G=0.986A=0.013
The Genome Aggregation DatabaseOtherSub300G=1.000A=0.000
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.979A=0.020
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
rs169860050.000106alcohol dependence21314694

eQTL of rs16986005 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 rs16986005 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 )
chr204034614640346220E0695024
chr204034630840346454E0695186
chr204034657140346737E0695449
chr204034252740342644E0701405
chr204034277440342849E0701652
chr204034303140343081E0701909
chr204034315540343230E0702033
chr204034614640346220E0705024
chr204034630840346454E0705186
chr204034657140346737E0705449
chr204034695740347010E0705835
chr204036726940367849E07126147
chr204036788240367960E07126760
chr204034695740347010E0825835




Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr204032109040322781E067-18341
chr204032109040322781E068-18341
chr204032109040322781E069-18341
chr204032109040322781E070-18341
chr204032109040322781E071-18341
chr204032109040322781E072-18341
chr204032109040322781E073-18341
chr204032109040322781E074-18341
chr204032109040322781E081-18341
chr204032109040322781E082-18341