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rs606231340

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231340(C;T)
Make rs606231340(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424143
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231340
ebirs606231340
HLIrs606231340
Exacrs606231340
Varsomers606231340
Maprs606231340
PheGenIrs606231340
hapmaprs606231340
1000 genomesrs606231340
hgdprs606231340
ensemblrs606231340
gopubmedrs606231340
geneviewrs606231340
scholarrs606231340
googlers606231340
pharmgkbrs606231340
gwascentralrs606231340
openSNPrs606231340
23andMers606231340
23andMe allrs606231340
SNP Nexus

SNPshotrs606231340
SNPdbers606231340
MSV3drs606231340
GWAS Ctlgrs606231340
Max Magnitude0
ClinVar
Risk rs606231340(T;T)
Alt rs606231340(T;T)
Reference rs606231340(C;C)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23893352C>T
CLNSRC
CLNACC RCV000148955.1,