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rs869025431

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025431(C;C)
Make rs869025431(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position136209946
GeneFHL1
is asnp
is mentioned by
dbSNPrs869025431
ebirs869025431
HLIrs869025431
Exacrs869025431
Varsomers869025431
Maprs869025431
PheGenIrs869025431
hapmaprs869025431
1000 genomesrs869025431
hgdprs869025431
ensemblrs869025431
gopubmedrs869025431
geneviewrs869025431
scholarrs869025431
googlers869025431
pharmgkbrs869025431
gwascentralrs869025431
openSNPrs869025431
23andMers869025431
23andMe allrs869025431
SNP Nexus

SNPshotrs869025431
SNPdbers869025431
MSV3drs869025431
GWAS Ctlgrs869025431
Max Magnitude0
ClinVar
Risk rs869025431(C;C)
Alt rs869025431(C;C)
Reference rs869025431(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene FHL1
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000023.10:g.135292105G>C
CLNSRC
CLNACC RCV000208197.1,