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rs730880732

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880732(A;G)
Make rs730880732(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426039
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880732
ebirs730880732
HLIrs730880732
Exacrs730880732
Varsomers730880732
Maprs730880732
PheGenIrs730880732
hapmaprs730880732
1000 genomesrs730880732
hgdprs730880732
ensemblrs730880732
gopubmedrs730880732
geneviewrs730880732
scholarrs730880732
googlers730880732
pharmgkbrs730880732
gwascentralrs730880732
openSNPrs730880732
23andMers730880732
23andMe allrs730880732
SNP Nexus

SNPshotrs730880732
SNPdbers730880732
MSV3drs730880732
GWAS Ctlgrs730880732
Max Magnitude0
ClinVar
Risk rs730880732(G;G)
Alt rs730880732(G;G)
Reference rs730880732(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23895248T>C
CLNSRC
CLNACC RCV000158507.2,