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rs587777097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777097(A;A)
Make rs587777097(A;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position128636991
GeneWDR34
is asnp
is mentioned by
dbSNPrs587777097
ebirs587777097
HLIrs587777097
Exacrs587777097
Varsomers587777097
Maprs587777097
PheGenIrs587777097
hapmaprs587777097
1000 genomesrs587777097
hgdprs587777097
ensemblrs587777097
gopubmedrs587777097
geneviewrs587777097
scholarrs587777097
googlers587777097
pharmgkbrs587777097
gwascentralrs587777097
openSNPrs587777097
23andMers587777097
23andMe allrs587777097
SNP Nexus

SNPshotrs587777097
SNPdbers587777097
MSV3drs587777097
GWAS Ctlgrs587777097
Max Magnitude0
ClinVar
Risk rs587777097(A;A)
Alt rs587777097(A;A)
Reference rs587777097(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.131399270G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000083290.3,