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rs1891320

From SNPedia

Orientationplus
Stabilizedplus
Make rs1891320(C;C)
Make rs1891320(C;T)
Make rs1891320(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position19970618
is asnp
is mentioned by
dbSNPrs1891320
dbSNP (classic)rs1891320
ClinGenrs1891320
ebirs1891320
HLIrs1891320
Exacrs1891320
Gnomadrs1891320
Varsomers1891320
LitVarrs1891320
Maprs1891320
PheGenIrs1891320
Biobankrs1891320
1000 genomesrs1891320
hgdprs1891320
ensemblrs1891320
geneviewrs1891320
scholarrs1891320
googlers1891320
pharmgkbrs1891320
gwascentralrs1891320
openSNPrs1891320
23andMers1891320
SNPshotrs1891320
SNPdbers1891320
MSV3drs1891320
GWAS Ctlgrs1891320
GMAF0.185
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20463618OA-icon.png] Role of polymorphic variants as genetic modulators of infection in neonatal sepsis