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rs7691216

From SNPedia

Orientationplus
Stabilizedplus
Make rs7691216(G;G)
Make rs7691216(G;T)
Make rs7691216(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position85208463
GeneARHGAP24
is asnp
is mentioned by
dbSNPrs7691216
dbSNP (classic)rs7691216
ClinGenrs7691216
ebirs7691216
HLIrs7691216
Exacrs7691216
Gnomadrs7691216
Varsomers7691216
LitVarrs7691216
Maprs7691216
PheGenIrs7691216
Biobankrs7691216
1000 genomesrs7691216
hgdprs7691216
ensemblrs7691216
geneviewrs7691216
scholarrs7691216
googlers7691216
pharmgkbrs7691216
gwascentralrs7691216
openSNPrs7691216
23andMers7691216
SNPshotrs7691216
SNPdbers7691216
MSV3drs7691216
GWAS Ctlgrs7691216
GMAF0.2383
Max Magnitude0
? (G;G) (G;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 G
P-val 7E-6
Odds Ratio .19 [0.11-0.27] unit decrease