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rs4150642

From SNPedia

Orientationplus
Stabilizedplus
Make rs4150642(C;C)
Make rs4150642(C;G)
Make rs4150642(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position18349351
GeneGTF2H1, LOC105376577
is asnp
is mentioned by
dbSNPrs4150642
ebirs4150642
HLIrs4150642
Exacrs4150642
Varsomers4150642
Maprs4150642
PheGenIrs4150642
hapmaprs4150642
1000 genomesrs4150642
hgdprs4150642
ensemblrs4150642
gopubmedrs4150642
geneviewrs4150642
scholarrs4150642
googlers4150642
pharmgkbrs4150642
gwascentralrs4150642
openSNPrs4150642
23andMers4150642
23andMe allrs4150642
SNP Nexus

SNPshotrs4150642
SNPdbers4150642
MSV3drs4150642
GWAS Ctlgrs4150642
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21124955OA-icon.png]
Trait Amyloid A serum levels
Title Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
Risk Allele G
P-val 3E-111
Odds Ratio .36 [0.26-0.46] unit increase