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rs587782990

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782990(G;G)
Make rs587782990(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position103026402
GeneCOL11A1
is asnp
is mentioned by
dbSNPrs587782990
ebirs587782990
HLIrs587782990
Exacrs587782990
Varsomers587782990
Maprs587782990
PheGenIrs587782990
hapmaprs587782990
1000 genomesrs587782990
hgdprs587782990
ensemblrs587782990
gopubmedrs587782990
geneviewrs587782990
scholarrs587782990
googlers587782990
pharmgkbrs587782990
gwascentralrs587782990
openSNPrs587782990
23andMers587782990
23andMe allrs587782990
SNP Nexus

SNPshotrs587782990
SNPdbers587782990
MSV3drs587782990
GWAS Ctlgrs587782990
Max Magnitude0
ClinVar
Risk rs587782990(G;G)
Alt rs587782990(G;G)
Reference rs587782990(T;T)
Significance Pathogenic
Disease sporadic abdominal aortic aneurysm
Variation info
Gene COL11A1
CLNDBN sporadic abdominal aortic aneurysm
Reversed 1
HGVS NC_000001.10:g.103491958A>C
CLNSRC
CLNACC RCV000144033.2,