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rs786205435

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205435(A;T)
Make rs786205435(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position15732617
GeneMYH11
is asnp
is mentioned by
dbSNPrs786205435
ebirs786205435
HLIrs786205435
Exacrs786205435
Varsomers786205435
Maprs786205435
PheGenIrs786205435
hapmaprs786205435
1000 genomesrs786205435
hgdprs786205435
ensemblrs786205435
gopubmedrs786205435
geneviewrs786205435
scholarrs786205435
googlers786205435
pharmgkbrs786205435
gwascentralrs786205435
openSNPrs786205435
23andMers786205435
23andMe allrs786205435
SNP Nexus

SNPshotrs786205435
SNPdbers786205435
MSV3drs786205435
GWAS Ctlgrs786205435
Max Magnitude0
ClinVar
Risk rs786205435(T;T)
Alt rs786205435(T;T)
Reference rs786205435(A;A)
Significance Probable-Pathogenic
Disease Visceral myopathy
Variation info
Gene MYH11
CLNDBN Visceral myopathy
Reversed 1
HGVS NC_000016.9:g.15826474T>A
CLNSRC Hospital Sainte-Justine
CLNACC RCV000172830.1,