rs11524
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs11524(C;C) |
Make rs11524(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 11826191 |
Gene | LPIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs11524 |
dbSNP (classic) | rs11524 |
ClinGen | rs11524 |
ebi | rs11524 |
HLI | rs11524 |
Exac | rs11524 |
Gnomad | rs11524 |
Varsome | rs11524 |
LitVar | rs11524 |
Map | rs11524 |
PheGenI | rs11524 |
Biobank | rs11524 |
1000 genomes | rs11524 |
hgdp | rs11524 |
ensembl | rs11524 |
geneview | rs11524 |
scholar | rs11524 |
rs11524 | |
pharmgkb | rs11524 |
gwascentral | rs11524 |
openSNP | rs11524 |
23andMe | rs11524 |
SNPshot | rs11524 |
SNPdbe | rs11524 |
MSV3d | rs11524 |
GWAS Ctlg | rs11524 |
GMAF | 0.2158 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
This SNP is postulated to be responsible for the lower blood pressure seen associated with SNP rs10495584, but direct evidence has not been found.[PMID 18437145]
ClinVar | |
---|---|
Risk | rs11524(C;C) |
Alt | rs11524(C;C) |
Reference | Rs11524(T;T) |
Significance | Non-pathogenic |
Disease | Acute Recurrent Myoglobinuria |
Variation | info |
Gene | LPIN1 |
CLNDBN | Acute Recurrent Myoglobinuria |
Reversed | 0 |
HGVS | NC_000002.11:g.11966317T>C |
CLNSRC | |
CLNACC | RCV000363530.1, |