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rs587777064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777064(C;T)
Make rs587777064(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position158918839
GeneWDR60
is asnp
is mentioned by
dbSNPrs587777064
ebirs587777064
HLIrs587777064
Exacrs587777064
Varsomers587777064
Maprs587777064
PheGenIrs587777064
hapmaprs587777064
1000 genomesrs587777064
hgdprs587777064
ensemblrs587777064
gopubmedrs587777064
geneviewrs587777064
scholarrs587777064
googlers587777064
pharmgkbrs587777064
gwascentralrs587777064
openSNPrs587777064
23andMers587777064
23andMe allrs587777064
SNP Nexus

SNPshotrs587777064
SNPdbers587777064
MSV3drs587777064
GWAS Ctlgrs587777064
Max Magnitude0
ClinVar
Risk rs587777064(T;T)
Alt rs587777064(T;T)
Reference rs587777064(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.158711530C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074338.4,