rs6923608

Homo sapiens
G>A / G>C
PRDM1 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0186 (5584/29948,GnomAD)
A=0195 (976/5008,1000G)
A=0149 (574/3854,ALSPAC)
A=0152 (565/3708,TWINSUK)
chr6:106089915 (GRCh38.p7) (6q21)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.106089915G>A
GRCh38.p7 chr 6NC_000006.12:g.106089915G>C
GRCh37.p13 chr 6NC_000006.11:g.106537790G>A
GRCh37.p13 chr 6NC_000006.11:g.106537790G>C
PRDM1 RefSeqGeneNG_029115.1:g.8596G>A
PRDM1 RefSeqGeneNG_029115.1:g.8596G>C

Gene: PRDM1, PR domain 1(plus strand)

Molecule type Change Amino acid[Codon] SO Term
PRDM1 transcript variant 1NM_001198.3:c.N/AIntron Variant
PRDM1 transcript variant 2NM_182907.2:c.N/AGenic Upstream Transcript Variant
PRDM1 transcript variant X2XM_006715550.3:c.N/AIntron Variant
PRDM1 transcript variant X1XM_011536062.2:c.N/AIntron Variant
PRDM1 transcript variant X3XM_011536063.2:c.N/AIntron Variant
PRDM1 transcript variant X5XM_017011187.1:c.N/AIntron Variant
PRDM1 transcript variant X4XM_011536064.2:c.N/AGenic Upstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.604A=0.396
1000GenomesAmericanSub694G=0.900A=0.100
1000GenomesEast AsianSub1008G=0.802A=0.198
1000GenomesEuropeSub1006G=0.889A=0.111
1000GenomesGlobalStudy-wide5008G=0.805A=0.195
1000GenomesSouth AsianSub978G=0.930A=0.070
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.851A=0.149
The Genome Aggregation DatabaseAfricanSub8706G=0.646A=0.354
The Genome Aggregation DatabaseAmericanSub838G=0.920A=0.080
The Genome Aggregation DatabaseEast AsianSub1618G=0.769A=0.231
The Genome Aggregation DatabaseEuropeSub18484G=0.890A=0.109
The Genome Aggregation DatabaseGlobalStudy-wide29948G=0.813A=0.186
The Genome Aggregation DatabaseOtherSub302G=0.890A=0.110
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.848A=0.152
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
rs69236083.2E-05alcohol and nictotine co-dependence20158304

eQTL of rs6923608 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 rs6923608 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.