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rs587777066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777066(A;A)
Make rs587777066(A;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position158914230
GeneWDR60
is asnp
is mentioned by
dbSNPrs587777066
ebirs587777066
HLIrs587777066
Exacrs587777066
Varsomers587777066
Maprs587777066
PheGenIrs587777066
hapmaprs587777066
1000 genomesrs587777066
hgdprs587777066
ensemblrs587777066
gopubmedrs587777066
geneviewrs587777066
scholarrs587777066
googlers587777066
pharmgkbrs587777066
gwascentralrs587777066
openSNPrs587777066
23andMers587777066
23andMe allrs587777066
SNP Nexus

SNPshotrs587777066
SNPdbers587777066
MSV3drs587777066
GWAS Ctlgrs587777066
Max Magnitude0
ClinVar
Risk rs587777066(A,C;A,C)
Alt rs587777066(A,C;A,C)
Reference rs587777066(T;T)
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.158706921T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074340.3,