rs10042968

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0195 (5831/29892,GnomAD)
G=0222 (6476/29118,TOPMED)
G=0148 (743/5008,1000G)
G=0210 (809/3854,ALSPAC)
G=0216 (800/3708,TWINSUK)
chr5:63737891 (GRCh38.p7) (5q12.2)
ND
GWASdb2 | GWASCatalog
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.63737891A>G
GRCh37.p13 chr 5NC_000005.9:g.63033718A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.741G=0.259
1000GenomesAmericanSub694A=0.850G=0.150
1000GenomesEast AsianSub1008A=0.984G=0.016
1000GenomesEuropeSub1006A=0.803G=0.197
1000GenomesGlobalStudy-wide5008A=0.852G=0.148
1000GenomesSouth AsianSub978A=0.920G=0.080
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.790G=0.210
The Genome Aggregation DatabaseAfricanSub8708A=0.763G=0.237
The Genome Aggregation DatabaseAmericanSub834A=0.840G=0.160
The Genome Aggregation DatabaseEast AsianSub1580A=0.967G=0.033
The Genome Aggregation DatabaseEuropeSub18468A=0.809G=0.190
The Genome Aggregation DatabaseGlobalStudy-wide29892A=0.804G=0.195
The Genome Aggregation DatabaseOtherSub302A=0.780G=0.220
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.777G=0.222
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.784G=0.216
PMID Title Author Journal
23216389Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence.Zuo LAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs100429680.0000008alcohol and nictotine co-dependence23216389
rs100429688.00E-07alcohol and nicotine co-dependence23216389

eQTL of rs10042968 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 rs10042968 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 )
chr56306788663067974E08134168
chr56306808263068414E08134364
chr56306847763068538E08134759
chr56298376762983849E082-49869
chr56298385462983965E082-49753
chr56298405762984141E082-49577