Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231318

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231318(A;A)
Make rs606231318(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429812
GeneMYH7
is asnp
is mentioned by
dbSNPrs606231318
ebirs606231318
HLIrs606231318
Exacrs606231318
Varsomers606231318
Maprs606231318
PheGenIrs606231318
hapmaprs606231318
1000 genomesrs606231318
hgdprs606231318
ensemblrs606231318
gopubmedrs606231318
geneviewrs606231318
scholarrs606231318
googlers606231318
pharmgkbrs606231318
gwascentralrs606231318
openSNPrs606231318
23andMers606231318
23andMe allrs606231318
SNP Nexus

SNPshotrs606231318
SNPdbers606231318
MSV3drs606231318
GWAS Ctlgrs606231318
Max Magnitude0
ClinVar
Risk rs606231318(A;A)
Alt rs606231318(A;A)
Reference rs606231318(C;C)
Significance Probable-Pathogenic
Disease Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN Familial cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23899021C>A
CLNSRC
CLNACC RCV000148980.1,