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

rs485499

From SNPedia

Orientationplus
Stabilizedplus
Make rs485499(C;C)
Make rs485499(C;T)
Make rs485499(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position160028076
GeneIL12A-AS1, LINC01100
is asnp
is mentioned by
dbSNPrs485499
ebirs485499
HLIrs485499
Exacrs485499
Varsomers485499
Maprs485499
PheGenIrs485499
hapmaprs485499
1000 genomesrs485499
hgdprs485499
ensemblrs485499
gopubmedrs485499
geneviewrs485499
scholarrs485499
googlers485499
pharmgkbrs485499
gwascentralrs485499
openSNPrs485499
23andMers485499
23andMe allrs485499
SNP Nexus

SNPshotrs485499
SNPdbers485499
MSV3drs485499
GWAS Ctlgrs485499
GMAF0.2241
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21399635OA-icon.png]
Trait
Title Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Risk Allele T
P-val 2E-16
Odds Ratio 1.3800 [1.28-1.50]