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rs587777092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777092(A;A)
Make rs587777092(A;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position128634842
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777092
ebirs587777092
HLIrs587777092
Exacrs587777092
Varsomers587777092
Maprs587777092
PheGenIrs587777092
hapmaprs587777092
1000 genomesrs587777092
hgdprs587777092
ensemblrs587777092
gopubmedrs587777092
geneviewrs587777092
scholarrs587777092
googlers587777092
pharmgkbrs587777092
gwascentralrs587777092
openSNPrs587777092
23andMers587777092
23andMe allrs587777092
SNP Nexus

SNPshotrs587777092
SNPdbers587777092
MSV3drs587777092
GWAS Ctlgrs587777092
Max Magnitude0
ClinVar
Risk rs587777092(A;A)
Alt rs587777092(A;A)
Reference rs587777092(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.131397121G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000083284.3,