Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777091(A;A)
Make rs587777091(A;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position128634881
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777091
ebirs587777091
HLIrs587777091
Exacrs587777091
Varsomers587777091
Maprs587777091
PheGenIrs587777091
hapmaprs587777091
1000 genomesrs587777091
hgdprs587777091
ensemblrs587777091
gopubmedrs587777091
geneviewrs587777091
scholarrs587777091
googlers587777091
pharmgkbrs587777091
gwascentralrs587777091
openSNPrs587777091
23andMers587777091
23andMe allrs587777091
SNP Nexus

SNPshotrs587777091
SNPdbers587777091
MSV3drs587777091
GWAS Ctlgrs587777091
Max Magnitude0
ClinVar
Risk rs587777091(A;A)
Alt rs587777091(A;A)
Reference rs587777091(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.131397160G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000083283.3,