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rs111404182

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111404182(C;T)
Make rs111404182(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position15750191
GeneMYH11
is asnp
is mentioned by
dbSNPrs111404182
ebirs111404182
HLIrs111404182
Exacrs111404182
Varsomers111404182
Maprs111404182
PheGenIrs111404182
hapmaprs111404182
1000 genomesrs111404182
hgdprs111404182
ensemblrs111404182
gopubmedrs111404182
geneviewrs111404182
scholarrs111404182
googlers111404182
pharmgkbrs111404182
gwascentralrs111404182
openSNPrs111404182
23andMers111404182
23andMe allrs111404182
SNP Nexus

SNPshotrs111404182
SNPdbers111404182
MSV3drs111404182
GWAS Ctlgrs111404182
Max Magnitude0
ClinVar
Risk rs111404182(A,T;A,T)
Alt rs111404182(A,T;A,T)
Reference rs111404182(C;C)
Significance Pathogenic
Disease Aortic aneurysm
Variation info
Gene MYH11
CLNDBN Aortic aneurysm, familial thoracic 4
Reversed 1
HGVS NC_000016.9:g.15844048G>A
CLNSRC
CLNACC RCV000148694.2,