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rs606231331

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231331(-;-)
Make rs606231331(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426793
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231331
ebirs606231331
HLIrs606231331
Exacrs606231331
Varsomers606231331
Maprs606231331
PheGenIrs606231331
hapmaprs606231331
1000 genomesrs606231331
hgdprs606231331
ensemblrs606231331
gopubmedrs606231331
geneviewrs606231331
scholarrs606231331
googlers606231331
pharmgkbrs606231331
gwascentralrs606231331
openSNPrs606231331
23andMers606231331
23andMe allrs606231331
SNP Nexus

SNPshotrs606231331
SNPdbers606231331
MSV3drs606231331
GWAS Ctlgrs606231331
Max Magnitude0
ClinVar
Risk rs606231331(;)
Alt rs606231331(;)
Reference rs606231331(A;A)
Significance Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23896002delA
CLNSRC
CLNACC RCV000148966.1,