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rs752881223

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs752881223(A;G)
Make rs752881223(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position65558307
GeneAXIN2
is asnp
is mentioned by
dbSNPrs752881223
ebirs752881223
HLIrs752881223
Exacrs752881223
Varsomers752881223
Maprs752881223
PheGenIrs752881223
hapmaprs752881223
1000 genomesrs752881223
hgdprs752881223
ensemblrs752881223
gopubmedrs752881223
geneviewrs752881223
scholarrs752881223
googlers752881223
pharmgkbrs752881223
gwascentralrs752881223
openSNPrs752881223
23andMers752881223
23andMe allrs752881223
SNP Nexus

SNPshotrs752881223
SNPdbers752881223
MSV3drs752881223
GWAS Ctlgrs752881223
Max Magnitude0
ClinVar
Risk rs752881223(G;G)
Alt rs752881223(G;G)
Reference rs752881223(A;A)
Significance Pathogenic
Disease Non-syndromic oligodontia
Variation info
Gene AXIN2
CLNDBN Non-syndromic oligodontia
Reversed 0
HGVS NC_000017.10:g.63554425A>C
CLNSRC
CLNACC RCV000201305.2,