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rs730880834

From SNPedia

Orientationminus
Stabilizedminus
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
dbSNP (classic)rs730880834
ClinGenrs730880834
ebirs730880834
HLIrs730880834
Exacrs730880834
Gnomadrs730880834
Varsomers730880834
LitVarrs730880834
Maprs730880834
PheGenIrs730880834
Biobankrs730880834
1000 genomesrs730880834
hgdprs730880834
ensemblrs730880834
geneviewrs730880834
scholarrs730880834
googlers730880834
pharmgkbrs730880834
gwascentralrs730880834
openSNPrs730880834
23andMers730880834
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 RCV000223182.2,