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rs606231328

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231328(C;C)
Make rs606231328(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427244
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231328
ebirs606231328
HLIrs606231328
Exacrs606231328
Varsomers606231328
Maprs606231328
PheGenIrs606231328
hapmaprs606231328
1000 genomesrs606231328
hgdprs606231328
ensemblrs606231328
gopubmedrs606231328
geneviewrs606231328
scholarrs606231328
googlers606231328
pharmgkbrs606231328
gwascentralrs606231328
openSNPrs606231328
23andMers606231328
23andMe allrs606231328
SNP Nexus

SNPshotrs606231328
SNPdbers606231328
MSV3drs606231328
GWAS Ctlgrs606231328
Max Magnitude0
ClinVar
Risk rs606231328(C;C)
Alt rs606231328(C;C)
Reference rs606231328(T;T)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23896453T>C
CLNSRC
CLNACC RCV000148970.1,