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rs606231323

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231323(G;T)
Make rs606231323(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23428548
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231323
ebirs606231323
HLIrs606231323
Exacrs606231323
Varsomers606231323
Maprs606231323
PheGenIrs606231323
hapmaprs606231323
1000 genomesrs606231323
hgdprs606231323
ensemblrs606231323
gopubmedrs606231323
geneviewrs606231323
scholarrs606231323
googlers606231323
pharmgkbrs606231323
gwascentralrs606231323
openSNPrs606231323
23andMers606231323
23andMe allrs606231323
SNP Nexus

SNPshotrs606231323
SNPdbers606231323
MSV3drs606231323
GWAS Ctlgrs606231323
Max Magnitude0
ClinVar
Risk rs606231323(T;T)
Alt rs606231323(T;T)
Reference rs606231323(G;G)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23897757G>T
CLNSRC
CLNACC RCV000148975.1,