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

rs587777352

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777352(A;A)
Make rs587777352(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position39273062
GeneWDR19
is asnp
is mentioned by
dbSNPrs587777352
ebirs587777352
HLIrs587777352
Exacrs587777352
Varsomers587777352
Maprs587777352
PheGenIrs587777352
hapmaprs587777352
1000 genomesrs587777352
hgdprs587777352
ensemblrs587777352
gopubmedrs587777352
geneviewrs587777352
scholarrs587777352
googlers587777352
pharmgkbrs587777352
gwascentralrs587777352
openSNPrs587777352
23andMers587777352
23andMe allrs587777352
SNP Nexus

SNPshotrs587777352
SNPdbers587777352
MSV3drs587777352
GWAS Ctlgrs587777352
Max Magnitude0
ClinVar
Risk rs587777352(A;A)
Alt rs587777352(A;A)
Reference rs587777352(G;G)
Significance Pathogenic
Disease Senior-loken syndrome 8
Variation info
Gene WDR19
CLNDBN Senior-loken syndrome 8
Reversed 0
HGVS NC_000004.11:g.39274682G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000115015.3,