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rs794728672

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728672(C;C)
Make rs794728672(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position15776099
GeneMYH11
is asnp
is mentioned by
dbSNPrs794728672
ebirs794728672
HLIrs794728672
Exacrs794728672
Varsomers794728672
Maprs794728672
PheGenIrs794728672
hapmaprs794728672
1000 genomesrs794728672
hgdprs794728672
ensemblrs794728672
gopubmedrs794728672
geneviewrs794728672
scholarrs794728672
googlers794728672
pharmgkbrs794728672
gwascentralrs794728672
openSNPrs794728672
23andMers794728672
23andMe allrs794728672
SNP Nexus

SNPshotrs794728672
SNPdbers794728672
MSV3drs794728672
GWAS Ctlgrs794728672
Max Magnitude0
ClinVar
Risk rs794728672(C;C)
Alt rs794728672(C;C)
Reference rs794728672(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.15869956C>G
CLNSRC
CLNACC RCV000182548.1,