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rs730880160

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880160(A;A)
Make rs730880160(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427846
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880160
ebirs730880160
HLIrs730880160
Exacrs730880160
Varsomers730880160
Maprs730880160
PheGenIrs730880160
hapmaprs730880160
1000 genomesrs730880160
hgdprs730880160
ensemblrs730880160
gopubmedrs730880160
geneviewrs730880160
scholarrs730880160
googlers730880160
pharmgkbrs730880160
gwascentralrs730880160
openSNPrs730880160
23andMers730880160
23andMe allrs730880160
SNP Nexus

SNPshotrs730880160
SNPdbers730880160
MSV3drs730880160
GWAS Ctlgrs730880160
Max Magnitude0
ClinVar
Risk rs730880160(A;A)
Alt rs730880160(A;A)
Reference rs730880160(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23897055C>T
CLNSRC
CLNACC RCV000157357.1,