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rs730880900

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880900(C;C)
Make rs730880900(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424106
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880900
ebirs730880900
HLIrs730880900
Exacrs730880900
Varsomers730880900
Maprs730880900
PheGenIrs730880900
hapmaprs730880900
1000 genomesrs730880900
hgdprs730880900
ensemblrs730880900
gopubmedrs730880900
geneviewrs730880900
scholarrs730880900
googlers730880900
pharmgkbrs730880900
gwascentralrs730880900
openSNPrs730880900
23andMers730880900
23andMe allrs730880900
SNP Nexus

SNPshotrs730880900
SNPdbers730880900
MSV3drs730880900
GWAS Ctlgrs730880900
Max Magnitude0
ClinVar
Risk rs730880900(C;C)
Alt rs730880900(C;C)
Reference rs730880900(T;T)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23893315A>G
CLNSRC
CLNACC RCV000158849.1,