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rs606231315

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231315(C;T)
Make rs606231315(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431678
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231315
ebirs606231315
HLIrs606231315
Exacrs606231315
Varsomers606231315
Maprs606231315
PheGenIrs606231315
hapmaprs606231315
1000 genomesrs606231315
hgdprs606231315
ensemblrs606231315
gopubmedrs606231315
geneviewrs606231315
scholarrs606231315
googlers606231315
pharmgkbrs606231315
gwascentralrs606231315
openSNPrs606231315
23andMers606231315
23andMe allrs606231315
SNP Nexus

SNPshotrs606231315
SNPdbers606231315
MSV3drs606231315
GWAS Ctlgrs606231315
Max Magnitude0
ClinVar
Risk rs606231315(T;T)
Alt rs606231315(T;T)
Reference rs606231315(C;C)
Significance Probable-Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23900887C>T
CLNSRC
CLNACC RCV000148983.1,