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rs786205114

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205114(-;-)
Make rs786205114(-;A)
Make rs786205114(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position39255914
GeneWDR19
is asnp
is mentioned by
dbSNPrs786205114
ebirs786205114
HLIrs786205114
Exacrs786205114
Varsomers786205114
Maprs786205114
PheGenIrs786205114
hapmaprs786205114
1000 genomesrs786205114
hgdprs786205114
ensemblrs786205114
gopubmedrs786205114
geneviewrs786205114
scholarrs786205114
googlers786205114
pharmgkbrs786205114
gwascentralrs786205114
openSNPrs786205114
23andMers786205114
23andMe allrs786205114
SNP Nexus

SNPshotrs786205114
SNPdbers786205114
MSV3drs786205114
GWAS Ctlgrs786205114
Max Magnitude0
ClinVar
Risk rs786205114(A;A)
Alt rs786205114(A;A)
Reference rs786205114(;)
Significance Pathogenic
Disease Nephronophthisis 13
Variation info
Gene WDR19
CLNDBN Nephronophthisis 13
Reversed 0
HGVS NC_000004.11:g.39257534dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000023685.3,