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rs730880897

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880897(A;G)
Make rs730880897(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424974
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880897
ebirs730880897
HLIrs730880897
Exacrs730880897
Varsomers730880897
Maprs730880897
PheGenIrs730880897
hapmaprs730880897
1000 genomesrs730880897
hgdprs730880897
ensemblrs730880897
gopubmedrs730880897
geneviewrs730880897
scholarrs730880897
googlers730880897
pharmgkbrs730880897
gwascentralrs730880897
openSNPrs730880897
23andMers730880897
23andMe allrs730880897
SNP Nexus

SNPshotrs730880897
SNPdbers730880897
MSV3drs730880897
GWAS Ctlgrs730880897
Max Magnitude0
ClinVar
Risk rs730880897(G;G)
Alt rs730880897(G;G)
Reference rs730880897(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894183T>C
CLNSRC
CLNACC RCV000158843.1,