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rs730880802

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880802(A;C)
Make rs730880802(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416980
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880802
ebirs730880802
HLIrs730880802
Exacrs730880802
Varsomers730880802
Maprs730880802
PheGenIrs730880802
hapmaprs730880802
1000 genomesrs730880802
hgdprs730880802
ensemblrs730880802
gopubmedrs730880802
geneviewrs730880802
scholarrs730880802
googlers730880802
pharmgkbrs730880802
gwascentralrs730880802
openSNPrs730880802
23andMers730880802
23andMe allrs730880802
SNP Nexus

SNPshotrs730880802
SNPdbers730880802
MSV3drs730880802
GWAS Ctlgrs730880802
Max Magnitude0
ClinVar
Risk rs730880802(C;C)
Alt rs730880802(C;C)
Reference rs730880802(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23886189T>G
CLNSRC
CLNACC RCV000158662.1,