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

rs121908118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908118(G;T)
Make rs121908118(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position218890304
GeneWNT10A
is asnp
is mentioned by
dbSNPrs121908118
ebirs121908118
HLIrs121908118
Exacrs121908118
Varsomers121908118
Maprs121908118
PheGenIrs121908118
hapmaprs121908118
1000 genomesrs121908118
hgdprs121908118
ensemblrs121908118
gopubmedrs121908118
geneviewrs121908118
scholarrs121908118
googlers121908118
pharmgkbrs121908118
gwascentralrs121908118
openSNPrs121908118
23andMers121908118
23andMe allrs121908118
SNP Nexus

SNPshotrs121908118
SNPdbers121908118
MSV3drs121908118
GWAS Ctlgrs121908118
Max Magnitude0
OMIM606268
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908118(A,T;A,T)
Alt rs121908118(A,T;A,T)
Reference rs121908118(G;G)
Significance Pathogenic
Disease Odontoonychodermal dysplasia
Variation info
Gene WNT10A
CLNDBN Odontoonychodermal dysplasia
Reversed 0
HGVS NC_000002.11:g.219755026G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004714.2,