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rs587777096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777096(C;T)
Make rs587777096(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position128634726
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777096
ebirs587777096
HLIrs587777096
Exacrs587777096
Varsomers587777096
Maprs587777096
PheGenIrs587777096
hapmaprs587777096
1000 genomesrs587777096
hgdprs587777096
ensemblrs587777096
gopubmedrs587777096
geneviewrs587777096
scholarrs587777096
googlers587777096
pharmgkbrs587777096
gwascentralrs587777096
openSNPrs587777096
23andMers587777096
23andMe allrs587777096
SNP Nexus

SNPshotrs587777096
SNPdbers587777096
MSV3drs587777096
GWAS Ctlgrs587777096
Max Magnitude0
ClinVar
Risk rs587777096(T;T)
Alt rs587777096(T;T)
Reference rs587777096(C;C)
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.131397005C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000083288.3,