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rs606231319

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231319(G;T)
Make rs606231319(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429335
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231319
ebirs606231319
HLIrs606231319
Exacrs606231319
Varsomers606231319
Maprs606231319
PheGenIrs606231319
hapmaprs606231319
1000 genomesrs606231319
hgdprs606231319
ensemblrs606231319
gopubmedrs606231319
geneviewrs606231319
scholarrs606231319
googlers606231319
pharmgkbrs606231319
gwascentralrs606231319
openSNPrs606231319
23andMers606231319
23andMe allrs606231319
SNP Nexus

SNPshotrs606231319
SNPdbers606231319
MSV3drs606231319
GWAS Ctlgrs606231319
Max Magnitude0
ClinVar
Risk rs606231319(T;T)
Alt rs606231319(T;T)
Reference rs606231319(G;G)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23898544G>T
CLNSRC
CLNACC RCV000148979.1,