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

rs786204852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204852(A;A)
Make rs786204852(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position39189694
GeneWDR19
is asnp
is mentioned by
dbSNPrs786204852
ebirs786204852
HLIrs786204852
Exacrs786204852
Varsomers786204852
Maprs786204852
PheGenIrs786204852
hapmaprs786204852
1000 genomesrs786204852
hgdprs786204852
ensemblrs786204852
gopubmedrs786204852
geneviewrs786204852
scholarrs786204852
googlers786204852
pharmgkbrs786204852
gwascentralrs786204852
openSNPrs786204852
23andMers786204852
23andMe allrs786204852
SNP Nexus

SNPshotrs786204852
SNPdbers786204852
MSV3drs786204852
GWAS Ctlgrs786204852
Max Magnitude0
ClinVar
Risk rs786204852(A;A)
Alt rs786204852(A;A)
Reference rs786204852(T;T)
Significance Pathogenic
Disease Senior-loken syndrome 8
Variation info
Gene WDR19
CLNDBN Senior-loken syndrome 8
Reversed 0
HGVS NC_000004.11:g.39191314T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000169776.3,