rs13297480
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs13297480(C;C) |
Make rs13297480(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 13219571 |
Gene | MPDZ |
is a | snp |
is | mentioned by |
dbSNP | rs13297480 |
dbSNP (classic) | rs13297480 |
ClinGen | rs13297480 |
ebi | rs13297480 |
HLI | rs13297480 |
Exac | rs13297480 |
Gnomad | rs13297480 |
Varsome | rs13297480 |
LitVar | rs13297480 |
Map | rs13297480 |
PheGenI | rs13297480 |
Biobank | rs13297480 |
1000 genomes | rs13297480 |
hgdp | rs13297480 |
ensembl | rs13297480 |
geneview | rs13297480 |
scholar | rs13297480 |
rs13297480 | |
pharmgkb | rs13297480 |
gwascentral | rs13297480 |
openSNP | rs13297480 |
23andMe | rs13297480 |
SNPshot | rs13297480 |
SNPdbe | rs13297480 |
MSV3d | rs13297480 |
GWAS Ctlg | rs13297480 |
GMAF | 0.1079 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19175764] rs13297480(G) a specific high-risk haplotype (p = 0.006, maximum statistic p = 0.051) for alcoholism
ClinVar | |
---|---|
Risk | rs13297480(C;C) |
Alt | rs13297480(C;C) |
Reference | Rs13297480(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | MPDZ |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000009.11:g.13219570T>C |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000146368.1, |