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

rs12750249

From SNPedia

Orientationplus
Stabilizedplus
Make rs12750249(C;C)
Make rs12750249(C;T)
Make rs12750249(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position94256104
GeneARHGAP29, LOC107985092
is asnp
is mentioned by
dbSNPrs12750249
dbSNP (classic)rs12750249
ClinGenrs12750249
ebirs12750249
HLIrs12750249
Exacrs12750249
Gnomadrs12750249
Varsomers12750249
LitVarrs12750249
Maprs12750249
PheGenIrs12750249
Biobankrs12750249
1000 genomesrs12750249
hgdprs12750249
ensemblrs12750249
geneviewrs12750249
scholarrs12750249
googlers12750249
pharmgkbrs12750249
gwascentralrs12750249
openSNPrs12750249
23andMers12750249
SNPshotrs12750249
SNPdbers12750249
MSV3drs12750249
GWAS Ctlgrs12750249
GMAF0.2236
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23382691OA-icon.png]
Trait IgG glycosylation
Title Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Risk Allele C
P-val 4E-6
Odds Ratio .17 [0.095-0.235] unit decrease