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rs730880813

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880813(A;G)
Make rs730880813(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415409
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880813
ebirs730880813
HLIrs730880813
Exacrs730880813
Varsomers730880813
Maprs730880813
PheGenIrs730880813
hapmaprs730880813
1000 genomesrs730880813
hgdprs730880813
ensemblrs730880813
gopubmedrs730880813
geneviewrs730880813
scholarrs730880813
googlers730880813
pharmgkbrs730880813
gwascentralrs730880813
openSNPrs730880813
23andMers730880813
23andMe allrs730880813
SNP Nexus

SNPshotrs730880813
SNPdbers730880813
MSV3drs730880813
GWAS Ctlgrs730880813
Max Magnitude0
ClinVar
Risk rs730880813(G;G)
Alt rs730880813(G;G)
Reference rs730880813(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23884618T>C
CLNSRC
CLNACC RCV000158689.1,