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rs606231332

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231332(A;C)
Make rs606231332(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426075
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231332
ebirs606231332
HLIrs606231332
Exacrs606231332
Varsomers606231332
Maprs606231332
PheGenIrs606231332
hapmaprs606231332
1000 genomesrs606231332
hgdprs606231332
ensemblrs606231332
gopubmedrs606231332
geneviewrs606231332
scholarrs606231332
googlers606231332
pharmgkbrs606231332
gwascentralrs606231332
openSNPrs606231332
23andMers606231332
23andMe allrs606231332
SNP Nexus

SNPshotrs606231332
SNPdbers606231332
MSV3drs606231332
GWAS Ctlgrs606231332
Max Magnitude0
ClinVar
Risk rs606231332(C,G;C,G)
Alt rs606231332(C,G;C,G)
Reference rs606231332(A;A)
Significance Pathogenic
Disease Familial cardiomyopathy not specified
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy not specified
Reversed 0
HGVS NC_000014.8:g.23895284A>C; NC_000014.8:g.23895284A>G
CLNSRC
CLNACC RCV000148965.1, RCV000158504.1,