Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777351(A;A)
Make rs587777351(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position39274945
GeneWDR19
is asnp
is mentioned by
dbSNPrs587777351
ebirs587777351
HLIrs587777351
Exacrs587777351
Varsomers587777351
Maprs587777351
PheGenIrs587777351
hapmaprs587777351
1000 genomesrs587777351
hgdprs587777351
ensemblrs587777351
gopubmedrs587777351
geneviewrs587777351
scholarrs587777351
googlers587777351
pharmgkbrs587777351
gwascentralrs587777351
openSNPrs587777351
23andMers587777351
23andMe allrs587777351
SNP Nexus

SNPshotrs587777351
SNPdbers587777351
MSV3drs587777351
GWAS Ctlgrs587777351
Max Magnitude0
ClinVar
Risk rs587777351(A;A)
Alt rs587777351(A;A)
Reference rs587777351(G;G)
Significance Pathogenic
Disease Nephronophthisis 13
Variation info
Gene WDR19
CLNDBN Nephronophthisis 13
Reversed 0
HGVS NC_000004.11:g.39276565G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000115013.3,