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rs587777350

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777350(C;T)
Make rs587777350(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position39205232
GeneWDR19
is asnp
is mentioned by
dbSNPrs587777350
ebirs587777350
HLIrs587777350
Exacrs587777350
Varsomers587777350
Maprs587777350
PheGenIrs587777350
hapmaprs587777350
1000 genomesrs587777350
hgdprs587777350
ensemblrs587777350
gopubmedrs587777350
geneviewrs587777350
scholarrs587777350
googlers587777350
pharmgkbrs587777350
gwascentralrs587777350
openSNPrs587777350
23andMers587777350
23andMe allrs587777350
SNP Nexus

SNPshotrs587777350
SNPdbers587777350
MSV3drs587777350
GWAS Ctlgrs587777350
Max Magnitude0
ClinVar
Risk rs587777350(T;T)
Alt rs587777350(T;T)
Reference rs587777350(C;C)
Significance Pathogenic
Disease Nephronophthisis 13
Variation info
Gene WDR19
CLNDBN Nephronophthisis 13
Reversed 0
HGVS NC_000004.11:g.39206852C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000115012.3,