rs1035961

Homo sapiens
A>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0061 (1836/29952,GnomAD)
C=0059 (1732/29118,TOPMED)
C=0132 (662/5008,1000G)
C=0068 (262/3854,ALSPAC)
C=0070 (258/3708,TWINSUK)
chr5:9928750 (GRCh38.p7) (5p15.2)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.9928750A>C
GRCh37.p13 chr 5NC_000005.9:g.9928862A>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.979C=0.021
1000GenomesAmericanSub694A=0.860C=0.140
1000GenomesEast AsianSub1008A=0.781C=0.219
1000GenomesEuropeSub1006A=0.945C=0.055
1000GenomesGlobalStudy-wide5008A=0.868C=0.132
1000GenomesSouth AsianSub978A=0.740C=0.260
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.932C=0.068
The Genome Aggregation DatabaseAfricanSub8718A=0.967C=0.033
The Genome Aggregation DatabaseAmericanSub838A=0.850C=0.150
The Genome Aggregation DatabaseEast AsianSub1604A=0.809C=0.191
The Genome Aggregation DatabaseEuropeSub18490A=0.940C=0.059
The Genome Aggregation DatabaseGlobalStudy-wide29952A=0.938C=0.061
The Genome Aggregation DatabaseOtherSub302A=0.910C=0.090
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.940C=0.059
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.930C=0.070
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
rs10359611.8E-06alcohol and nictotine co-dependence20158304

eQTL of rs1035961 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 rs1035961 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.