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rs730880918

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880918(C;T)
Make rs730880918(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23413763
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880918
ebirs730880918
HLIrs730880918
Exacrs730880918
Varsomers730880918
Maprs730880918
PheGenIrs730880918
hapmaprs730880918
1000 genomesrs730880918
hgdprs730880918
ensemblrs730880918
gopubmedrs730880918
geneviewrs730880918
scholarrs730880918
googlers730880918
pharmgkbrs730880918
gwascentralrs730880918
openSNPrs730880918
23andMers730880918
23andMe allrs730880918
SNP Nexus

SNPshotrs730880918
SNPdbers730880918
MSV3drs730880918
GWAS Ctlgrs730880918
Max Magnitude0
ClinVar
Risk rs730880918(T;T)
Alt rs730880918(T;T)
Reference rs730880918(C;C)
Significance Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23882972G>A
CLNSRC
CLNACC RCV000168923.1, RCV000208216.1,