rs9314995

Homo sapiens
G>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0352 (10427/29624,GnomAD)
T=0363 (10570/29116,TOPMED)
T=0338 (1695/5008,1000G)
T=0358 (1380/3854,ALSPAC)
T=0339 (1257/3708,TWINSUK)
chr13:30070281 (GRCh38.p7) (13q12.3)
ND
GWASdb2
1   publication(s)
See rs on genome
53 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.30070281G>T
GRCh37.p13 chr 13NC_000013.10:g.30644418G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.594T=0.406
1000GenomesAmericanSub694G=0.560T=0.440
1000GenomesEast AsianSub1008G=0.776T=0.224
1000GenomesEuropeSub1006G=0.655T=0.345
1000GenomesGlobalStudy-wide5008G=0.662T=0.338
1000GenomesSouth AsianSub978G=0.710T=0.290
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.642T=0.358
The Genome Aggregation DatabaseAfricanSub8644G=0.591T=0.409
The Genome Aggregation DatabaseAmericanSub830G=0.590T=0.410
The Genome Aggregation DatabaseEast AsianSub1610G=0.780T=0.220
The Genome Aggregation DatabaseEuropeSub18238G=0.664T=0.335
The Genome Aggregation DatabaseGlobalStudy-wide29624G=0.648T=0.352
The Genome Aggregation DatabaseOtherSub302G=0.780T=0.220
Trans-Omics for Precision MedicineGlobalStudy-wide29116G=0.637T=0.363
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.661T=0.339
PMID Title Author Journal
20158304A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations.Lind PATwin Res Hum Genet

P-Value

SNP ID p-value Traits Study
rs93149955.05E-05alcohol and nictotine co-dependence20158304

eQTL of rs9314995 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 rs9314995 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 )
chr133060704530607120E067-37298
chr133060721530607259E067-37159
chr133060727330607323E067-37095
chr133060737730607427E067-36991
chr133060769230609127E067-35291
chr133068655230686633E06742134
chr133068671530690207E06742297
chr133059939530599455E068-44963
chr133059961230599684E068-44734
chr133060737730607427E068-36991
chr133060769230609127E068-35291
chr133062794730628487E068-15931
chr133068655230686633E06842134
chr133060656630606616E069-37802
chr133060667230606722E069-37696
chr133060704530607120E069-37298
chr133060721530607259E069-37159
chr133060727330607323E069-37095
chr133060737730607427E069-36991
chr133060769230609127E069-35291
chr133068584330686514E06941425
chr133068655230686633E06942134
chr133068671530690207E06942297
chr133068136430682066E07036946
chr133068283930683509E07038421
chr133068671530690207E07042297
chr133069027530690574E07045857
chr133069062530690774E07046207
chr133060721530607259E071-37159
chr133060727330607323E071-37095
chr133060737730607427E071-36991
chr133060769230609127E071-35291
chr133064587930647454E0711461
chr133068584330686514E07141425
chr133068671530690207E07142297
chr133060656630606616E072-37802
chr133060667230606722E072-37696
chr133060704530607120E072-37298
chr133060721530607259E072-37159
chr133060727330607323E072-37095
chr133060737730607427E072-36991
chr133068584330686514E07241425
chr133060769230609127E074-35291
chr133064587930647454E0741461
chr133068655230686633E07442134
chr133068663630686677E07442218
chr133068671530690207E07442297
chr133061148830611771E081-32647
chr133061188930612282E081-32136
chr133068283930683509E08138421
chr133068655230686633E08142134
chr133068663630686677E08142218
chr133068671530690207E08142297