Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908123

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908123(A;A)
Make rs121908123(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position218881022
GeneWNT10A
is asnp
is mentioned by
dbSNPrs121908123
ebirs121908123
HLIrs121908123
Exacrs121908123
Varsomers121908123
Maprs121908123
PheGenIrs121908123
hapmaprs121908123
1000 genomesrs121908123
hgdprs121908123
ensemblrs121908123
gopubmedrs121908123
geneviewrs121908123
scholarrs121908123
googlers121908123
pharmgkbrs121908123
gwascentralrs121908123
openSNPrs121908123
23andMers121908123
23andMe allrs121908123
SNP Nexus

SNPshotrs121908123
SNPdbers121908123
MSV3drs121908123
GWAS Ctlgrs121908123
Max Magnitude0
OMIM606268
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908123(A;A)
Alt rs121908123(A;A)
Reference rs121908123(G;G)
Significance Pathogenic
Disease Odontoonychodermal dysplasia
Variation info
Gene WNT10A
CLNDBN Odontoonychodermal dysplasia
Reversed 0
HGVS NC_000002.11:g.219745744G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004720.2,