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rs1063320

From SNPedia

Orientationminus
Stabilizedminus
Make rs1063320(C;C)
Make rs1063320(C;G)
Make rs1063320(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29830972
GeneHLA-G
is asnp
is mentioned by
dbSNPrs1063320
ebirs1063320
HLIrs1063320
Exacrs1063320
Varsomers1063320
Maprs1063320
PheGenIrs1063320
hapmaprs1063320
1000 genomesrs1063320
hgdprs1063320
ensemblrs1063320
gopubmedrs1063320
geneviewrs1063320
scholarrs1063320
googlers1063320
pharmgkbrs1063320
gwascentralrs1063320
openSNPrs1063320
23andMers1063320
23andMe allrs1063320
SNP Nexus

SNPshotrs1063320
SNPdbers1063320
MSV3drs1063320
GWAS Ctlgrs1063320
GMAF0.4481
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 19775370] HLA-G polymorphism influences the susceptibility to HCV infection in sickle cell disease patients


[PMID 20070604] The 3'-untranslated region of the HLA-G gene in relation to pre-eclampsia: revisited


[PMID 20593013OA-icon.png] A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01.


[PMID 21395561] Association of the HLA-G gene +3142C>G polymorphism with systemic lupus erythematosus.


[PMID 23238918] Genome-wide pathway analysis of a genome-wide association study on multiple sclerosis.


[PMID 25637667] Human leukocyte antigen (HLA)-G during pregnancy part II: Associations between maternal and fetal HLA-G genotypes and soluble HLA-G


[PMID 26889902] Immunogenetics of prostate cancer and benign hyperplasia - the potential use of an HLA-G variant as a tag SNP for prostate cancer risk.


[PMID 27664842] 14-bp ins/del polymorphism and +3142C>G SNP of the HLA-G gene have a significant impact on acute rejection after liver transplantation.