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rs3892630

From SNPedia

Orientationplus
Stabilizedplus
Make rs3892630(C;C)
Make rs3892630(C;T)
Make rs3892630(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position32690578
GeneNUDT19
is asnp
is mentioned by
dbSNPrs3892630
dbSNP (classic)rs3892630
ClinGenrs3892630
ebirs3892630
HLIrs3892630
Exacrs3892630
Gnomadrs3892630
Varsomers3892630
LitVarrs3892630
Maprs3892630
PheGenIrs3892630
Biobankrs3892630
1000 genomesrs3892630
hgdprs3892630
ensemblrs3892630
geneviewrs3892630
scholarrs3892630
googlers3892630
pharmgkbrs3892630
gwascentralrs3892630
openSNPrs3892630
23andMers3892630
SNPshotrs3892630
SNPdbers3892630
MSV3drs3892630
GWAS Ctlgrs3892630
GMAF0.1993
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele T
P-val 1E-10
Odds Ratio .18 [0.11-0.24] unit increase