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rs121908568

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908568(C;T)
Make rs121908568(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position65536495
GeneAXIN2
is asnp
is mentioned by
dbSNPrs121908568
ebirs121908568
HLIrs121908568
Exacrs121908568
Varsomers121908568
Maprs121908568
PheGenIrs121908568
hapmaprs121908568
1000 genomesrs121908568
hgdprs121908568
ensemblrs121908568
gopubmedrs121908568
geneviewrs121908568
scholarrs121908568
googlers121908568
pharmgkbrs121908568
gwascentralrs121908568
openSNPrs121908568
23andMers121908568
23andMe allrs121908568
SNP Nexus

SNPshotrs121908568
SNPdbers121908568
MSV3drs121908568
GWAS Ctlgrs121908568
Max Magnitude0
OMIM604025
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908568(T;T)
Alt rs121908568(T;T)
Reference rs121908568(C;C)
Significance Pathogenic
Disease Oligodontia-colorectal cancer syndrome
Variation info
Gene AXIN2
CLNDBN Oligodontia-colorectal cancer syndrome
Reversed 1
HGVS NC_000017.10:g.63532613G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006239.3,