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rs2716601

From SNPedia

Orientationminus
Stabilizedminus
Make rs2716601(C;C)
Make rs2716601(C;T)
Make rs2716601(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position74042353
is asnp
is mentioned by
dbSNPrs2716601
ebirs2716601
HLIrs2716601
Exacrs2716601
Varsomers2716601
Maprs2716601
PheGenIrs2716601
hapmaprs2716601
1000 genomesrs2716601
hgdprs2716601
ensemblrs2716601
gopubmedrs2716601
geneviewrs2716601
scholarrs2716601
googlers2716601
pharmgkbrs2716601
gwascentralrs2716601
openSNPrs2716601
23andMers2716601
23andMe allrs2716601
SNP Nexus

SNPshotrs2716601
SNPdbers2716601
MSV3drs2716601
GWAS Ctlgrs2716601
GMAF0.4348
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22310353]
Trait
Title Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis.
Risk Allele
P-val 0.000001
Odds Ratio None None