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rs730880903

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880903(C;T)
Make rs730880903(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422268
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880903
ebirs730880903
HLIrs730880903
Exacrs730880903
Varsomers730880903
Maprs730880903
PheGenIrs730880903
hapmaprs730880903
1000 genomesrs730880903
hgdprs730880903
ensemblrs730880903
gopubmedrs730880903
geneviewrs730880903
scholarrs730880903
googlers730880903
pharmgkbrs730880903
gwascentralrs730880903
openSNPrs730880903
23andMers730880903
23andMe allrs730880903
SNP Nexus

SNPshotrs730880903
SNPdbers730880903
MSV3drs730880903
GWAS Ctlgrs730880903
Max Magnitude0
ClinVar
Risk rs730880903(T;T)
Alt rs730880903(T;T)
Reference rs730880903(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23891477G>A
CLNSRC
CLNACC RCV000158857.1,