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rs730882193

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882193(A;A)
Make rs730882193(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position65536472
GeneAXIN2
is asnp
is mentioned by
dbSNPrs730882193
ebirs730882193
HLIrs730882193
Exacrs730882193
Varsomers730882193
Maprs730882193
PheGenIrs730882193
hapmaprs730882193
1000 genomesrs730882193
hgdprs730882193
ensemblrs730882193
gopubmedrs730882193
geneviewrs730882193
scholarrs730882193
googlers730882193
pharmgkbrs730882193
gwascentralrs730882193
openSNPrs730882193
23andMers730882193
23andMe allrs730882193
SNP Nexus

SNPshotrs730882193
SNPdbers730882193
MSV3drs730882193
GWAS Ctlgrs730882193
Max Magnitude0
ClinVar
Risk rs730882193(A;A)
Alt rs730882193(A;A)
Reference rs730882193(G;G)
Significance Pathogenic
Disease Oligodontia-colorectal cancer syndrome
Variation info
Gene AXIN2
CLNDBN Oligodontia-colorectal cancer syndrome
Reversed 1
HGVS NC_000017.10:g.63532590C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033255.4,