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rs606231324

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231324(C;T)
Make rs606231324(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23428505
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231324
ebirs606231324
HLIrs606231324
Exacrs606231324
Varsomers606231324
Maprs606231324
PheGenIrs606231324
hapmaprs606231324
1000 genomesrs606231324
hgdprs606231324
ensemblrs606231324
gopubmedrs606231324
geneviewrs606231324
scholarrs606231324
googlers606231324
pharmgkbrs606231324
gwascentralrs606231324
openSNPrs606231324
23andMers606231324
23andMe allrs606231324
SNP Nexus

SNPshotrs606231324
SNPdbers606231324
MSV3drs606231324
GWAS Ctlgrs606231324
Max Magnitude0
ClinVar
Risk rs606231324(T;T)
Alt rs606231324(T;T)
Reference rs606231324(C;C)
Significance Pathogenic
Disease Familial cardiomyopathy Cardiomyopathy Left ventricular noncompaction cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy Cardiomyopathy Left ventricular noncompaction cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23897714C>T
CLNSRC
CLNACC RCV000148974.1, RCV000154447.2, RCV000157356.1,