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rs606231335

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231335(A;G)
Make rs606231335(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425807
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231335
ebirs606231335
HLIrs606231335
Exacrs606231335
Varsomers606231335
Maprs606231335
PheGenIrs606231335
hapmaprs606231335
1000 genomesrs606231335
hgdprs606231335
ensemblrs606231335
gopubmedrs606231335
geneviewrs606231335
scholarrs606231335
googlers606231335
pharmgkbrs606231335
gwascentralrs606231335
openSNPrs606231335
23andMers606231335
23andMe allrs606231335
SNP Nexus

SNPshotrs606231335
SNPdbers606231335
MSV3drs606231335
GWAS Ctlgrs606231335
Max Magnitude0
ClinVar
Risk rs606231335(G;G)
Alt rs606231335(G;G)
Reference rs606231335(A;A)
Significance Probable-Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23895016A>G
CLNSRC
CLNACC RCV000148961.1,