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rs121908899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908899(A;A)
Make rs121908899(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position112064842
GeneWISP3
is asnp
is mentioned by
dbSNPrs121908899
ebirs121908899
HLIrs121908899
Exacrs121908899
Varsomers121908899
Maprs121908899
PheGenIrs121908899
hapmaprs121908899
1000 genomesrs121908899
hgdprs121908899
ensemblrs121908899
gopubmedrs121908899
geneviewrs121908899
scholarrs121908899
googlers121908899
pharmgkbrs121908899
gwascentralrs121908899
openSNPrs121908899
23andMers121908899
23andMe allrs121908899
SNP Nexus

SNPshotrs121908899
SNPdbers121908899
MSV3drs121908899
GWAS Ctlgrs121908899
Max Magnitude0
OMIM603400
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908899(A;A)
Alt rs121908899(A;A)
Reference rs121908899(G;G)
Significance Pathogenic
Disease Progressive pseudorheumatoid dysplasia
Variation info
Gene WISP3
CLNDBN Progressive pseudorheumatoid dysplasia
Reversed 0
HGVS NC_000006.11:g.112386045G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006751.3,