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rs121908567

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908567(G;T)
Make rs121908567(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position65536345
GeneAXIN2
is asnp
is mentioned by
dbSNPrs121908567
ebirs121908567
HLIrs121908567
Exacrs121908567
Varsomers121908567
Maprs121908567
PheGenIrs121908567
hapmaprs121908567
1000 genomesrs121908567
hgdprs121908567
ensemblrs121908567
gopubmedrs121908567
geneviewrs121908567
scholarrs121908567
googlers121908567
pharmgkbrs121908567
gwascentralrs121908567
openSNPrs121908567
23andMers121908567
23andMe allrs121908567
SNP Nexus

SNPshotrs121908567
SNPdbers121908567
MSV3drs121908567
GWAS Ctlgrs121908567
Max Magnitude0
OMIM604025
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908567(T;T)
Alt rs121908567(T;T)
Reference rs121908567(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene AXIN2
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000017.10:g.63532463C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006237.4,