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rs587777095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777095(G;G)
Make rs587777095(G;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position128634923
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777095
ebirs587777095
HLIrs587777095
Exacrs587777095
Varsomers587777095
Maprs587777095
PheGenIrs587777095
hapmaprs587777095
1000 genomesrs587777095
hgdprs587777095
ensemblrs587777095
gopubmedrs587777095
geneviewrs587777095
scholarrs587777095
googlers587777095
pharmgkbrs587777095
gwascentralrs587777095
openSNPrs587777095
23andMers587777095
23andMe allrs587777095
SNP Nexus

SNPshotrs587777095
SNPdbers587777095
MSV3drs587777095
GWAS Ctlgrs587777095
Max Magnitude0
ClinVar
Risk rs587777095(G;G)
Alt rs587777095(G;G)
Reference rs587777095(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.131397202T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000083287.4,