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rs606231321

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231321(C;T)
Make rs606231321(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429095
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231321
ebirs606231321
HLIrs606231321
Exacrs606231321
Varsomers606231321
Maprs606231321
PheGenIrs606231321
hapmaprs606231321
1000 genomesrs606231321
hgdprs606231321
ensemblrs606231321
gopubmedrs606231321
geneviewrs606231321
scholarrs606231321
googlers606231321
pharmgkbrs606231321
gwascentralrs606231321
openSNPrs606231321
23andMers606231321
23andMe allrs606231321
SNP Nexus

SNPshotrs606231321
SNPdbers606231321
MSV3drs606231321
GWAS Ctlgrs606231321
Max Magnitude0
ClinVar
Risk rs606231321(T;T)
Alt rs606231321(T;T)
Reference rs606231321(C;C)
Significance Probable-Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23898304C>T
CLNSRC
CLNACC RCV000148977.1,