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rs11524

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11524(C;C)
Make rs11524(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position11826191
GeneLPIN1
is asnp
is mentioned by
dbSNPrs11524
dbSNP (classic)rs11524
ClinGenrs11524
ebirs11524
HLIrs11524
Exacrs11524
Gnomadrs11524
Varsomers11524
LitVarrs11524
Maprs11524
PheGenIrs11524
Biobankrs11524
1000 genomesrs11524
hgdprs11524
ensemblrs11524
geneviewrs11524
scholarrs11524
googlers11524
pharmgkbrs11524
gwascentralrs11524
openSNPrs11524
23andMers11524
SNPshotrs11524
SNPdbers11524
MSV3drs11524
GWAS Ctlgrs11524
GMAF0.2158
Max Magnitude0
? (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,