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rs587777093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777093(A;A)
Make rs587777093(A;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position128634259
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777093
ebirs587777093
HLIrs587777093
Exacrs587777093
Varsomers587777093
Maprs587777093
PheGenIrs587777093
hapmaprs587777093
1000 genomesrs587777093
hgdprs587777093
ensemblrs587777093
gopubmedrs587777093
geneviewrs587777093
scholarrs587777093
googlers587777093
pharmgkbrs587777093
gwascentralrs587777093
openSNPrs587777093
23andMers587777093
23andMe allrs587777093
SNP Nexus

SNPshotrs587777093
SNPdbers587777093
MSV3drs587777093
GWAS Ctlgrs587777093
Max Magnitude0
ClinVar
Risk rs587777093(A;A)
Alt rs587777093(A;A)
Reference rs587777093(G;G)
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.131396538G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000083285.3,