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rs606231334

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231334(C;T)
Make rs606231334(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425819
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231334
ebirs606231334
HLIrs606231334
Exacrs606231334
Varsomers606231334
Maprs606231334
PheGenIrs606231334
hapmaprs606231334
1000 genomesrs606231334
hgdprs606231334
ensemblrs606231334
gopubmedrs606231334
geneviewrs606231334
scholarrs606231334
googlers606231334
pharmgkbrs606231334
gwascentralrs606231334
openSNPrs606231334
23andMers606231334
23andMe allrs606231334
SNP Nexus

SNPshotrs606231334
SNPdbers606231334
MSV3drs606231334
GWAS Ctlgrs606231334
Max Magnitude0
ClinVar
Risk rs606231334(A,T;A,T)
Alt rs606231334(A,T;A,T)
Reference rs606231334(C;C)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23895028C>T
CLNSRC
CLNACC RCV000148963.1,