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rs606231337

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231337(-;-)
Make rs606231337(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425339
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231337
ebirs606231337
HLIrs606231337
Exacrs606231337
Varsomers606231337
Maprs606231337
PheGenIrs606231337
hapmaprs606231337
1000 genomesrs606231337
hgdprs606231337
ensemblrs606231337
gopubmedrs606231337
geneviewrs606231337
scholarrs606231337
googlers606231337
pharmgkbrs606231337
gwascentralrs606231337
openSNPrs606231337
23andMers606231337
23andMe allrs606231337
SNP Nexus

SNPshotrs606231337
SNPdbers606231337
MSV3drs606231337
GWAS Ctlgrs606231337
Max Magnitude0
ClinVar
Risk rs606231337(;)
Alt rs606231337(;)
Reference rs606231337(T;T)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23894548delT
CLNSRC
CLNACC RCV000148959.1,