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rs387906983

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906983(G;G)
Make rs387906983(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position39215913
GeneWDR19
is asnp
is mentioned by
dbSNPrs387906983
ebirs387906983
HLIrs387906983
Exacrs387906983
Varsomers387906983
Maprs387906983
PheGenIrs387906983
hapmaprs387906983
1000 genomesrs387906983
hgdprs387906983
ensemblrs387906983
gopubmedrs387906983
geneviewrs387906983
scholarrs387906983
googlers387906983
pharmgkbrs387906983
gwascentralrs387906983
openSNPrs387906983
23andMers387906983
23andMe allrs387906983
SNP Nexus

SNPshotrs387906983
SNPdbers387906983
MSV3drs387906983
GWAS Ctlgrs387906983
Max Magnitude0
ClinVar
Risk rs387906983(G;G)
Alt rs387906983(G;G)
Reference rs387906983(T;T)
Significance Pathogenic
Disease Nephronophthisis 13
Variation info
Gene WDR19
CLNDBN Nephronophthisis 13
Reversed 0
HGVS NC_000004.11:g.39217533T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023684.3,