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

rs121908900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908900(A;A)
Make rs121908900(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position112069548
GeneWISP3
is asnp
is mentioned by
dbSNPrs121908900
ebirs121908900
HLIrs121908900
Exacrs121908900
Varsomers121908900
Maprs121908900
PheGenIrs121908900
hapmaprs121908900
1000 genomesrs121908900
hgdprs121908900
ensemblrs121908900
gopubmedrs121908900
geneviewrs121908900
scholarrs121908900
googlers121908900
pharmgkbrs121908900
gwascentralrs121908900
openSNPrs121908900
23andMers121908900
23andMe allrs121908900
SNP Nexus

SNPshotrs121908900
SNPdbers121908900
MSV3drs121908900
GWAS Ctlgrs121908900
Max Magnitude0
OMIM603400
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908900(A;A)
Alt rs121908900(A;A)
Reference rs121908900(G;G)
Significance Pathogenic
Disease Progressive pseudorheumatoid dysplasia
Variation info
Gene WISP3
CLNDBN Progressive pseudorheumatoid dysplasia
Reversed 0
HGVS NC_000006.11:g.112390751G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006752.3,