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rs751386429

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs751386429(A;A)
Make rs751386429(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position39253193
GeneWDR19
is asnp
is mentioned by
dbSNPrs751386429
ebirs751386429
HLIrs751386429
Exacrs751386429
Varsomers751386429
Maprs751386429
PheGenIrs751386429
hapmaprs751386429
1000 genomesrs751386429
hgdprs751386429
ensemblrs751386429
gopubmedrs751386429
geneviewrs751386429
scholarrs751386429
googlers751386429
pharmgkbrs751386429
gwascentralrs751386429
openSNPrs751386429
23andMers751386429
23andMe allrs751386429
SNP Nexus

SNPshotrs751386429
SNPdbers751386429
MSV3drs751386429
GWAS Ctlgrs751386429
Max Magnitude0
ClinVar
Risk rs751386429(A;A)
Alt rs751386429(A;A)
Reference rs751386429(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WDR19
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.39254813G>T
CLNSRC
CLNACC RCV000171376.1,