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rs606231316

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231316(A;A)
Make rs606231316(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429840
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231316
ebirs606231316
HLIrs606231316
Exacrs606231316
Varsomers606231316
Maprs606231316
PheGenIrs606231316
hapmaprs606231316
1000 genomesrs606231316
hgdprs606231316
ensemblrs606231316
gopubmedrs606231316
geneviewrs606231316
scholarrs606231316
googlers606231316
pharmgkbrs606231316
gwascentralrs606231316
openSNPrs606231316
23andMers606231316
23andMe allrs606231316
SNP Nexus

SNPshotrs606231316
SNPdbers606231316
MSV3drs606231316
GWAS Ctlgrs606231316
Max Magnitude0
ClinVar
Risk rs606231316(A;A)
Alt rs606231316(A;A)
Reference rs606231316(T;T)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23899049T>A
CLNSRC
CLNACC RCV000148982.1,