Have questions? Visit https://www.reddit.com/r/SNPedia

rs1829975

From SNPedia

Orientationminus
Stabilizedminus
Make rs1829975(A;A)
Make rs1829975(A;G)
Make rs1829975(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position160928658
is asnp
is mentioned by
dbSNPrs1829975
ebirs1829975
HLIrs1829975
Exacrs1829975
Varsomers1829975
Maprs1829975
PheGenIrs1829975
hapmaprs1829975
1000 genomesrs1829975
hgdprs1829975
ensemblrs1829975
gopubmedrs1829975
geneviewrs1829975
scholarrs1829975
googlers1829975
pharmgkbrs1829975
gwascentralrs1829975
openSNPrs1829975
23andMers1829975
23andMe allrs1829975
SNP Nexus

SNPshotrs1829975
SNPdbers1829975
MSV3drs1829975
GWAS Ctlgrs1829975
GMAF0.2277
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio None None