rs16911018

Homo sapiens
G>A / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
A=0096 (2899/29952,GnomAD)
A=0119 (3488/29118,TOPMED)
A=0129 (648/5008,1000G)
A=0060 (233/3854,ALSPAC)
A=0070 (260/3708,TWINSUK)
chr10:130632855 (GRCh38.p7) (10q26.3)
AD
GWASdb2
1   publication(s)
See rs on genome
107 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 10NC_000010.11:g.130632855G>A
GRCh38.p7 chr 10NC_000010.11:g.130632855G>T
GRCh37.p13 chr 10NC_000010.10:g.132431119G>A
GRCh37.p13 chr 10NC_000010.10:g.132431119G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.765A=0.235
1000GenomesAmericanSub694G=0.910A=0.090
1000GenomesEast AsianSub1008G=0.891A=0.109
1000GenomesEuropeSub1006G=0.955A=0.045
1000GenomesGlobalStudy-wide5008G=0.871A=0.129
1000GenomesSouth AsianSub978G=0.880A=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.940A=0.060
The Genome Aggregation DatabaseAfricanSub8714G=0.792A=0.208
The Genome Aggregation DatabaseAmericanSub838G=0.940A=0.060
The Genome Aggregation DatabaseEast AsianSub1616G=0.893A=0.107
The Genome Aggregation DatabaseEuropeSub18482G=0.953A=0.046
The Genome Aggregation DatabaseGlobalStudy-wide29952G=0.903A=0.096
The Genome Aggregation DatabaseOtherSub302G=0.960A=0.040
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.880A=0.119
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.930A=0.070
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs169110180.000193alcohol dependence20201924

eQTL of rs16911018 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 rs16911018 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 )
chr101068464110685197E06716892
chr101068629010686669E06718541
chr101070841110708511E06740662
chr101070886810708954E06741119
chr101070919210709251E06741443
chr101070934610709466E06741597
chr101070957210709663E06741823
chr101068419110684620E06816442
chr101068606010686193E06818311
chr101070433410704571E06836585
chr101070760510707992E06839856
chr101070811310708167E06840364
chr101070934610709466E06841597
chr101070957210709663E06841823
chr101070973210709879E06841983
chr101070997310710045E06842224
chr101070433410704571E06936585
chr101068464110685197E07016892
chr101070466910705537E07036920
chr101070973210709879E07041983
chr101070997310710045E07042224
chr101065587010655924E071-11825
chr101065596310656187E071-11562
chr101065633710656450E071-11299
chr101068419110684620E07116442
chr101070466910705537E07136920
chr101070934610709466E07141597
chr101070957210709663E07141823
chr101070973210709879E07141983
chr101070400410704054E07236255
chr101070406210704141E07236313
chr101070433410704571E07236585
chr101066538710665550E073-2199
chr101066564510665694E073-2055
chr101066581810665949E073-1800
chr101066599610666968E073-781
chr101068406010684110E07316311
chr101068419110684620E07316442
chr101068713810687267E07319389
chr101070811310708167E07340364
chr101070433410704571E07436585
chr101070466910705537E07436920
chr101063234610632397E081-35352
chr101063357910634529E081-33220
chr101064213210642224E081-25525
chr101065019310650243E081-17506
chr101065040910650473E081-17276
chr101065065910650753E081-16996
chr101065123310651848E081-15901
chr101065200510652828E081-14921
chr101065336610653416E081-14333
chr101065342110653523E081-14226
chr101066511210665217E081-2532
chr101066525810665337E081-2412
chr101066538710665550E081-2199
chr101066564510665694E081-2055
chr101066581810665949E081-1800
chr101066599610666968E081-781
chr101066729210667342E081-407
chr101066741010667464E081-285
chr101066857110668803E081822
chr101066881610668979E0811067
chr101067184410672583E0814095
chr101067281310673211E0815064
chr101067331610673379E0815567
chr101067417710674356E0816428
chr101067446410674514E0816715
chr101067458710674638E0816838
chr101068419110684620E08116442
chr101068464110685197E08116892
chr101068520910685428E08117460
chr101068827610688806E08120527
chr101070919210709251E08141443
chr101070934610709466E08141597
chr101070957210709663E08141823
chr101070973210709879E08141983
chr101070997310710045E08142224
chr101065123310651848E082-15901
chr101065587010655924E082-11825
chr101065596310656187E082-11562
chr101066511210665217E082-2532
chr101066525810665337E082-2412
chr101066538710665550E082-2199
chr101066564510665694E082-2055
chr101066581810665949E082-1800
chr101066599610666968E082-781
chr101066729210667342E082-407
chr101066857110668803E082822
chr101066881610668979E0821067
chr101066915710669408E0821408
chr101066954310669626E0821794
chr101067281310673211E0825064
chr101067331610673379E0825567
chr101067341210673504E0825663
chr101067359410673644E0825845
chr101067378810674053E0826039
chr101067417710674356E0826428
chr101067843310678487E08210684
chr101068419110684620E08216442
chr101068606010686193E08218311
chr101068629010686669E08218541
chr101068667410687135E08218925
chr101068713810687267E08219389
chr101070934610709466E08241597
chr101070957210709663E08241823
chr101070973210709879E08241983
chr101070997310710045E08242224