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rs606231322

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231322(C;T)
Make rs606231322(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429071
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231322
ebirs606231322
HLIrs606231322
Exacrs606231322
Varsomers606231322
Maprs606231322
PheGenIrs606231322
hapmaprs606231322
1000 genomesrs606231322
hgdprs606231322
ensemblrs606231322
gopubmedrs606231322
geneviewrs606231322
scholarrs606231322
googlers606231322
pharmgkbrs606231322
gwascentralrs606231322
openSNPrs606231322
23andMers606231322
23andMe allrs606231322
SNP Nexus

SNPshotrs606231322
SNPdbers606231322
MSV3drs606231322
GWAS Ctlgrs606231322
Max Magnitude0
ClinVar
Risk rs606231322(T;T)
Alt rs606231322(T;T)
Reference rs606231322(C;C)
Significance Probable-Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23898280C>T
CLNSRC
CLNACC RCV000148976.1,