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rs8046180

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs8046180(A;A)
Make rs8046180(A;C)
Make rs8046180(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position15721599
GeneMYH11, NDE1
is asnp
is mentioned by
dbSNPrs8046180
ebirs8046180
HLIrs8046180
Exacrs8046180
Varsomers8046180
Maprs8046180
PheGenIrs8046180
hapmaprs8046180
1000 genomesrs8046180
hgdprs8046180
ensemblrs8046180
gopubmedrs8046180
geneviewrs8046180
scholarrs8046180
googlers8046180
pharmgkbrs8046180
gwascentralrs8046180
openSNPrs8046180
23andMers8046180
23andMe allrs8046180
SNP Nexus

SNPshotrs8046180
SNPdbers8046180
MSV3drs8046180
GWAS Ctlgrs8046180
Max Magnitude0
ClinVar
Risk rs8046180(A,C;A,C)
Alt rs8046180(A,C;A,C)
Reference rs8046180(G;G)
Significance Pathogenic
Disease not specified Aortic aneurysm not provided
Variation info
Gene NDE1 MYH11
CLNDBN not specified Aortic aneurysm, familial thoracic 4 not provided
Reversed 0
HGVS NC_000016.9:g.15815456G>A; NC_000016.9:g.15815456G>C
CLNSRC
CLNACC RCV000126951.2, RCV000229335.1, RCV000182519.2,