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rs587777348

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587777348(-;T)
Make rs587777348(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position39205191
GeneWDR19
is asnp
is mentioned by
dbSNPrs587777348
dbSNP (classic)rs587777348
ClinGenrs587777348
ebirs587777348
HLIrs587777348
Exacrs587777348
Gnomadrs587777348
Varsomers587777348
LitVarrs587777348
Maprs587777348
PheGenIrs587777348
Biobankrs587777348
1000 genomesrs587777348
hgdprs587777348
ensemblrs587777348
geneviewrs587777348
scholarrs587777348
googlers587777348
pharmgkbrs587777348
gwascentralrs587777348
openSNPrs587777348
23andMers587777348
SNPshotrs587777348
SNPdbers587777348
MSV3drs587777348
GWAS Ctlgrs587777348
Max Magnitude0
ClinVar
Risk rs587777348(T;T)
Alt rs587777348(T;T)
Reference Rs587777348(-;-)
Significance Pathogenic
Disease Senior-Loken syndrome 8
Variation info
Gene WDR19
CLNDBN Senior-Loken syndrome 8
Reversed 0
HGVS NC_000004.11:g.39206811dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000115010.3,