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rs121908901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908901(A;A)
Make rs121908901(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position112061098
GeneWISP3
is asnp
is mentioned by
dbSNPrs121908901
ebirs121908901
HLIrs121908901
Exacrs121908901
Varsomers121908901
Maprs121908901
PheGenIrs121908901
hapmaprs121908901
1000 genomesrs121908901
hgdprs121908901
ensemblrs121908901
gopubmedrs121908901
geneviewrs121908901
scholarrs121908901
googlers121908901
pharmgkbrs121908901
gwascentralrs121908901
openSNPrs121908901
23andMers121908901
23andMe allrs121908901
SNP Nexus

SNPshotrs121908901
SNPdbers121908901
MSV3drs121908901
GWAS Ctlgrs121908901
Max Magnitude0
OMIM603400
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908901(A;A)
Alt rs121908901(A;A)
Reference rs121908901(C;C)
Significance Pathogenic
Disease Progressive pseudorheumatoid dysplasia
Variation info
Gene WISP3
CLNDBN Progressive pseudorheumatoid dysplasia
Reversed 0
HGVS NC_000006.11:g.112382301C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006753.3,