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rs79436363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs79436363(A;A)
Make rs79436363(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position39273029
GeneWDR19
is asnp
is mentioned by
dbSNPrs79436363
dbSNP (classic)rs79436363
ClinGenrs79436363
ebirs79436363
HLIrs79436363
Exacrs79436363
Gnomadrs79436363
Varsomers79436363
LitVarrs79436363
Maprs79436363
PheGenIrs79436363
Biobankrs79436363
1000 genomesrs79436363
hgdprs79436363
ensemblrs79436363
geneviewrs79436363
scholarrs79436363
googlers79436363
pharmgkbrs79436363
gwascentralrs79436363
openSNPrs79436363
23andMers79436363
SNPshotrs79436363
SNPdbers79436363
MSV3drs79436363
GWAS Ctlgrs79436363
Max Magnitude0
ClinVar
Risk rs79436363(A;A)
Alt rs79436363(A;A)
Reference Rs79436363(G;G)
Significance Pathogenic
Disease Senior-Loken syndrome 8 not provided
Variation info
Gene WDR19
CLNDBN Senior-Loken syndrome 8 not provided
Reversed 0
HGVS NC_000004.11:g.39274649G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000115014.3, RCV000433622.1,