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rs113186231

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113186231(C;G)
Make rs113186231(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427584
GeneMYH7
is asnp
is mentioned by
dbSNPrs113186231
ebirs113186231
HLIrs113186231
Exacrs113186231
Varsomers113186231
Maprs113186231
PheGenIrs113186231
hapmaprs113186231
1000 genomesrs113186231
hgdprs113186231
ensemblrs113186231
gopubmedrs113186231
geneviewrs113186231
scholarrs113186231
googlers113186231
pharmgkbrs113186231
gwascentralrs113186231
openSNPrs113186231
23andMers113186231
23andMe allrs113186231
SNP Nexus

SNPshotrs113186231
SNPdbers113186231
MSV3drs113186231
GWAS Ctlgrs113186231
Max Magnitude0
ClinVar
Risk rs113186231(G,T;G,T)
Alt rs113186231(G,T;G,T)
Reference rs113186231(C;C)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000014.8:g.23896793C>T
CLNSRC
CLNACC RCV000157367.1, RCV000158893.1,