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rs769688376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769688376(A;A)
Make rs769688376(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position36089289
GeneWDR62
is asnp
is mentioned by
dbSNPrs769688376
dbSNP (classic)rs769688376
ClinGenrs769688376
ebirs769688376
HLIrs769688376
Exacrs769688376
Gnomadrs769688376
Varsomers769688376
LitVarrs769688376
Maprs769688376
PheGenIrs769688376
Biobankrs769688376
1000 genomesrs769688376
hgdprs769688376
ensemblrs769688376
geneviewrs769688376
scholarrs769688376
googlers769688376
pharmgkbrs769688376
gwascentralrs769688376
openSNPrs769688376
23andMers769688376
SNPshotrs769688376
SNPdbers769688376
MSV3drs769688376
GWAS Ctlgrs769688376
Max Magnitude0
ClinVar
Risk rs769688376(A;A)
Alt rs769688376(A;A)
Reference Rs769688376(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene WDR62
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.36580191C>A
CLNSRC
CLNACC RCV000330039.1,