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

rs587776850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs587776850(-;-)
Make rs587776850(-;TCT)
Make rs587776850(TCT;TCT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position41224645
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs587776850
ClinGenrs587776850
ebirs587776850
HLIrs587776850
Exacrs587776850
Varsomers587776850
Maprs587776850
PheGenIrs587776850
hapmaprs587776850
1000 genomesrs587776850
hgdprs587776850
ensemblrs587776850
gopubmedrs587776850
geneviewrs587776850
scholarrs587776850
googlers587776850
pharmgkbrs587776850
gwascentralrs587776850
openSNPrs587776850
23andMers587776850
23andMe allrs587776850
SNP Nexus

SNPshotrs587776850
SNPdbers587776850
MSV3drs587776850
GWAS Ctlgrs587776850
Max Magnitude0
ClinVar
Risk rs587776850(-;-)
Alt rs587776850(-;-)
Reference Rs587776850(CTT;CTT)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene CTNNB1
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000003.11:g.41266136_41266138delTCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000019137.5,