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rs6000782

From SNPedia

Orientationplus
Stabilizedplus
Make rs6000782(A;A)
Make rs6000782(A;C)
Make rs6000782(C;C)
ReferenceGRCh38 38.1/142
Chromosome22
Position37532179
is asnp
is mentioned by
dbSNPrs6000782
ebirs6000782
HLIrs6000782
Exacrs6000782
Varsomers6000782
Maprs6000782
PheGenIrs6000782
hapmaprs6000782
1000 genomesrs6000782
hgdprs6000782
ensemblrs6000782
gopubmedrs6000782
geneviewrs6000782
scholarrs6000782
googlers6000782
pharmgkbrs6000782
gwascentralrs6000782
openSNPrs6000782
23andMers6000782
23andMe allrs6000782
SNP Nexus

SNPshotrs6000782
SNPdbers6000782
MSV3drs6000782
GWAS Ctlgrs6000782
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24768677]
Trait Autoimmune hepatitis type-1
Title Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.
Risk Allele
P-val 3E-6
Odds Ratio 1.70 [1.40-2.10]