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rs587777065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777065(C;T)
Make rs587777065(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position158923722
GeneWDR60
is asnp
is mentioned by
dbSNPrs587777065
ebirs587777065
HLIrs587777065
Exacrs587777065
Varsomers587777065
Maprs587777065
PheGenIrs587777065
hapmaprs587777065
1000 genomesrs587777065
hgdprs587777065
ensemblrs587777065
gopubmedrs587777065
geneviewrs587777065
scholarrs587777065
googlers587777065
pharmgkbrs587777065
gwascentralrs587777065
openSNPrs587777065
23andMers587777065
23andMe allrs587777065
SNP Nexus

SNPshotrs587777065
SNPdbers587777065
MSV3drs587777065
GWAS Ctlgrs587777065
Max Magnitude0
ClinVar
Risk rs587777065(T;T)
Alt rs587777065(T;T)
Reference rs587777065(C;C)
Significance Pathogenic
Disease Short-rib thoracic dysplasia 8 with or without polydactyly
Variation info
Gene WDR60
CLNDBN Short-rib thoracic dysplasia 8 with or without polydactyly
Reversed 0
HGVS NC_000007.13:g.158716413C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074339.4,