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rs142546324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142546324(C;T)
Make rs142546324(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position15718337
GeneMYH11, NDE1
is asnp
is mentioned by
dbSNPrs142546324
ebirs142546324
HLIrs142546324
Exacrs142546324
Varsomers142546324
Maprs142546324
PheGenIrs142546324
hapmaprs142546324
1000 genomesrs142546324
hgdprs142546324
ensemblrs142546324
gopubmedrs142546324
geneviewrs142546324
scholarrs142546324
googlers142546324
pharmgkbrs142546324
gwascentralrs142546324
openSNPrs142546324
23andMers142546324
23andMe allrs142546324
SNP Nexus

SNPshotrs142546324
SNPdbers142546324
MSV3drs142546324
GWAS Ctlgrs142546324
Max Magnitude0
ClinVar
Risk rs142546324(T;T)
Alt rs142546324(T;T)
Reference rs142546324(C;C)
Significance Pathogenic
Disease Aortic aneurysm not specified
Variation info
Gene NDE1 MYH11
CLNDBN Aortic aneurysm, familial thoracic 4 not specified
Reversed 0
HGVS NC_000016.9:g.15812194C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015192.25, RCV000148691.1, RCV000182528.1,