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rs587776642

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs587776642(-;-)
Make rs587776642(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position110638153
GeneBUB1
is asnp
is mentioned by
dbSNPrs587776642
ebirs587776642
HLIrs587776642
Exacrs587776642
Varsomers587776642
Maprs587776642
PheGenIrs587776642
hapmaprs587776642
1000 genomesrs587776642
hgdprs587776642
ensemblrs587776642
gopubmedrs587776642
geneviewrs587776642
scholarrs587776642
googlers587776642
pharmgkbrs587776642
gwascentralrs587776642
openSNPrs587776642
23andMers587776642
23andMe allrs587776642
SNP Nexus

SNPshotrs587776642
SNPdbers587776642
MSV3drs587776642
GWAS Ctlgrs587776642
Max Magnitude0
ClinVar
Risk rs587776642(AC,C;AC,C)
Alt rs587776642(AC,C;AC,C)
Reference rs587776642(TC;TC)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene BUB1
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000002.11:g.111395730delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007151.4,