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rs587777098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777098(C;C)
Make rs587777098(C;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position128634291
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777098
ebirs587777098
HLIrs587777098
Exacrs587777098
Varsomers587777098
Maprs587777098
PheGenIrs587777098
hapmaprs587777098
1000 genomesrs587777098
hgdprs587777098
ensemblrs587777098
gopubmedrs587777098
geneviewrs587777098
scholarrs587777098
googlers587777098
pharmgkbrs587777098
gwascentralrs587777098
openSNPrs587777098
23andMers587777098
23andMe allrs587777098
SNP Nexus

SNPshotrs587777098
SNPdbers587777098
MSV3drs587777098
GWAS Ctlgrs587777098
Max Magnitude0
ClinVar
Risk rs587777098(C;C)
Alt rs587777098(C;C)
Reference rs587777098(T;T)
Significance Pathogenic
Disease Short-rib thoracic dysplasia 11 with or without polydactyly
Variation info
Gene WDR34
CLNDBN Short-rib thoracic dysplasia 11 with or without polydactyly
Reversed 0
HGVS NC_000009.11:g.131396570T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000083291.4,