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rs193922629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922629(C;C)
Make rs193922629(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position15737509
GeneMYH11
is asnp
is mentioned by
dbSNPrs193922629
ebirs193922629
HLIrs193922629
Exacrs193922629
Varsomers193922629
Maprs193922629
PheGenIrs193922629
hapmaprs193922629
1000 genomesrs193922629
hgdprs193922629
ensemblrs193922629
gopubmedrs193922629
geneviewrs193922629
scholarrs193922629
googlers193922629
pharmgkbrs193922629
gwascentralrs193922629
openSNPrs193922629
23andMers193922629
23andMe allrs193922629
SNP Nexus

SNPshotrs193922629
SNPdbers193922629
MSV3drs193922629
GWAS Ctlgrs193922629
Max Magnitude0
ClinVar
Risk rs193922629(C;C)
Alt rs193922629(C;C)
Reference rs193922629(T;T)
Significance Probable-Pathogenic
Disease Familial aortopathy
Variation info
Gene MYH11
CLNDBN Familial aortopathy
Reversed 1
HGVS NC_000016.9:g.15831366A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030296.1,