rs728115

Homo sapiens
G>A
KCND2 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0148 (4448/29888,GnomAD)
A=0179 (895/5008,1000G)
A=0103 (397/3854,ALSPAC)
A=0092 (342/3708,TWINSUK)
chr7:120665095 (GRCh38.p7) (7q31.31)
ND
GWASdb2 | GWASCatalog
2   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.120665095G>A
GRCh37.p13 chr 7NC_000007.13:g.120305149G>A
KCND2 RefSeqGeneNG_034230.1:g.396428G>A

Gene: KCND2, potassium voltage-gated channel subfamily D member 2(plus strand)

Molecule type Change Amino acid[Codon] SO Term
KCND2 transcriptNM_012281.2:c.N/AIntron Variant
KCND2 transcript variant X1XM_011516165.2:c.N/AGenic Downstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.906A=0.094
1000GenomesAmericanSub694G=0.770A=0.230
1000GenomesEast AsianSub1008G=0.586A=0.414
1000GenomesEuropeSub1006G=0.896A=0.104
1000GenomesGlobalStudy-wide5008G=0.821A=0.179
1000GenomesSouth AsianSub978G=0.910A=0.090
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.897A=0.103
The Genome Aggregation DatabaseAfricanSub8714G=0.887A=0.113
The Genome Aggregation DatabaseAmericanSub838G=0.740A=0.260
The Genome Aggregation DatabaseEast AsianSub1612G=0.584A=0.416
The Genome Aggregation DatabaseEuropeSub18422G=0.862A=0.137
The Genome Aggregation DatabaseGlobalStudy-wide29888G=0.851A=0.148
The Genome Aggregation DatabaseOtherSub302G=0.850A=0.150
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.908A=0.092
PMID Title Author Journal
21956439Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.Zuo LNeuropsychopharmacology
22488850Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence.Zuo LAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs7281154E-06alcohol and nictotine co-dependence22488850

eQTL of rs728115 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 rs728115 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.