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rs730880154

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880154(A;A)
Make rs730880154(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23433131
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880154
ebirs730880154
HLIrs730880154
Exacrs730880154
Varsomers730880154
Maprs730880154
PheGenIrs730880154
hapmaprs730880154
1000 genomesrs730880154
hgdprs730880154
ensemblrs730880154
gopubmedrs730880154
geneviewrs730880154
scholarrs730880154
googlers730880154
pharmgkbrs730880154
gwascentralrs730880154
openSNPrs730880154
23andMers730880154
23andMe allrs730880154
SNP Nexus

SNPshotrs730880154
SNPdbers730880154
MSV3drs730880154
GWAS Ctlgrs730880154
Max Magnitude0
ClinVar
Risk rs730880154(A,T;A,T)
Alt rs730880154(A,T;A,T)
Reference rs730880154(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy, restrictive
Reversed 1
HGVS NC_000014.8:g.23902340C>T
CLNSRC
CLNACC RCV000157347.1,