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

rs121908902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908902(C;C)
Make rs121908902(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position112061174
GeneWISP3
is asnp
is mentioned by
dbSNPrs121908902
ebirs121908902
HLIrs121908902
Exacrs121908902
Varsomers121908902
Maprs121908902
PheGenIrs121908902
hapmaprs121908902
1000 genomesrs121908902
hgdprs121908902
ensemblrs121908902
gopubmedrs121908902
geneviewrs121908902
scholarrs121908902
googlers121908902
pharmgkbrs121908902
gwascentralrs121908902
openSNPrs121908902
23andMers121908902
23andMe allrs121908902
SNP Nexus

SNPshotrs121908902
SNPdbers121908902
MSV3drs121908902
GWAS Ctlgrs121908902
Max Magnitude0
OMIM603400
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908902(C;C)
Alt rs121908902(C;C)
Reference rs121908902(T;T)
Significance Pathogenic
Disease Progressive pseudorheumatoid dysplasia
Variation info
Gene WISP3
CLNDBN Progressive pseudorheumatoid dysplasia
Reversed 0
HGVS NC_000006.11:g.112382377T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006754.3,