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rs730880834

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880834(A;A)
Make rs730880834(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432710
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880834
ebirs730880834
HLIrs730880834
Exacrs730880834
Varsomers730880834
Maprs730880834
PheGenIrs730880834
hapmaprs730880834
1000 genomesrs730880834
hgdprs730880834
ensemblrs730880834
gopubmedrs730880834
geneviewrs730880834
scholarrs730880834
googlers730880834
pharmgkbrs730880834
gwascentralrs730880834
openSNPrs730880834
23andMers730880834
23andMe allrs730880834
SNP Nexus

SNPshotrs730880834
SNPdbers730880834
MSV3drs730880834
GWAS Ctlgrs730880834
Max Magnitude0
ClinVar
Risk rs730880834(A;A)
Alt rs730880834(A;A)
Reference rs730880834(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901919C>T
CLNSRC
CLNACC RCV000223182.1,