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rs1884596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1884596(C;C)
Make rs1884596(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position21923501
is asnp
is mentioned by
dbSNPrs1884596
dbSNP (classic)rs1884596
ClinGenrs1884596
ebirs1884596
HLIrs1884596
Exacrs1884596
Gnomadrs1884596
Varsomers1884596
LitVarrs1884596
Maprs1884596
PheGenIrs1884596
Biobankrs1884596
1000 genomesrs1884596
hgdprs1884596
ensemblrs1884596
geneviewrs1884596
scholarrs1884596
googlers1884596
pharmgkbrs1884596
gwascentralrs1884596
openSNPrs1884596
23andMers1884596
SNPshotrs1884596
SNPdbers1884596
MSV3drs1884596
GWAS Ctlgrs1884596
GMAF0.03949
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19907058] No evidence for association of the KLF12 gene with RA in a large UK cohort of >7,000 samples