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rs606231329

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231329(A;C)
Make rs606231329(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427238
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231329
ebirs606231329
HLIrs606231329
Exacrs606231329
Varsomers606231329
Maprs606231329
PheGenIrs606231329
hapmaprs606231329
1000 genomesrs606231329
hgdprs606231329
ensemblrs606231329
gopubmedrs606231329
geneviewrs606231329
scholarrs606231329
googlers606231329
pharmgkbrs606231329
gwascentralrs606231329
openSNPrs606231329
23andMers606231329
23andMe allrs606231329
SNP Nexus

SNPshotrs606231329
SNPdbers606231329
MSV3drs606231329
GWAS Ctlgrs606231329
Max Magnitude0
ClinVar
Risk rs606231329(C;C)
Alt rs606231329(C;C)
Reference rs606231329(A;A)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23896447A>C
CLNSRC
CLNACC RCV000148969.1,