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rs267606674

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606674(-;-)
Make rs267606674(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position65536467
GeneAXIN2
is asnp
is mentioned by
dbSNPrs267606674
ebirs267606674
HLIrs267606674
Exacrs267606674
Varsomers267606674
Maprs267606674
PheGenIrs267606674
hapmaprs267606674
1000 genomesrs267606674
hgdprs267606674
ensemblrs267606674
gopubmedrs267606674
geneviewrs267606674
scholarrs267606674
googlers267606674
pharmgkbrs267606674
gwascentralrs267606674
openSNPrs267606674
23andMers267606674
23andMe allrs267606674
SNP Nexus

SNPshotrs267606674
SNPdbers267606674
MSV3drs267606674
GWAS Ctlgrs267606674
Max Magnitude0
ClinVar
Risk rs267606674(;)
Alt rs267606674(;)
Reference rs267606674(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene AXIN2
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000017.10:g.63532585delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000006238.4,