Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909055

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909055(A;A)
Make rs121909055(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position110658451
GeneBUB1
is asnp
is mentioned by
dbSNPrs121909055
ebirs121909055
HLIrs121909055
Exacrs121909055
Varsomers121909055
Maprs121909055
PheGenIrs121909055
hapmaprs121909055
1000 genomesrs121909055
hgdprs121909055
ensemblrs121909055
gopubmedrs121909055
geneviewrs121909055
scholarrs121909055
googlers121909055
pharmgkbrs121909055
gwascentralrs121909055
openSNPrs121909055
23andMers121909055
23andMe allrs121909055
SNP Nexus

SNPshotrs121909055
SNPdbers121909055
MSV3drs121909055
GWAS Ctlgrs121909055
Max Magnitude0
OMIM602452
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909055(A;A)
Alt rs121909055(A;A)
Reference rs121909055(C;C)
Significance Pathogenic
Disease Colorectal cancer with chromosomal instability
Variation info
Gene BUB1 SNORD132
CLNDBN Colorectal cancer with chromosomal instability
Reversed 1
HGVS NC_000002.11:g.111416028G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007499.2,