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rs794729661

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729661(A;A)
Make rs794729661(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position110672660
GeneBUB1
is asnp
is mentioned by
dbSNPrs794729661
ebirs794729661
HLIrs794729661
Exacrs794729661
Varsomers794729661
Maprs794729661
PheGenIrs794729661
hapmaprs794729661
1000 genomesrs794729661
hgdprs794729661
ensemblrs794729661
gopubmedrs794729661
geneviewrs794729661
scholarrs794729661
googlers794729661
pharmgkbrs794729661
gwascentralrs794729661
openSNPrs794729661
23andMers794729661
23andMe allrs794729661
SNP Nexus

SNPshotrs794729661
SNPdbers794729661
MSV3drs794729661
GWAS Ctlgrs794729661
Max Magnitude0
ClinVar
Risk rs794729661(A;A)
Alt rs794729661(A;A)
Reference rs794729661(G;G)
Significance Pathogenic
Disease Colorectal cancer with chromosomal instability
Variation info
Gene BUB1
CLNDBN Colorectal cancer with chromosomal instability
Reversed 1
HGVS NC_000002.11:g.111430237C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007498.2,