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rs2068824

From SNPedia

Orientationminus
Stabilizedminus
Make rs2068824(A;A)
Make rs2068824(A;G)
Make rs2068824(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position201625537
GeneNAV1
is asnp
is mentioned by
dbSNPrs2068824
ebirs2068824
HLIrs2068824
Exacrs2068824
Varsomers2068824
Maprs2068824
PheGenIrs2068824
hapmaprs2068824
1000 genomesrs2068824
hgdprs2068824
ensemblrs2068824
gopubmedrs2068824
geneviewrs2068824
scholarrs2068824
googlers2068824
pharmgkbrs2068824
gwascentralrs2068824
openSNPrs2068824
23andMers2068824
23andMe allrs2068824
SNP Nexus

SNPshotrs2068824
SNPdbers2068824
MSV3drs2068824
GWAS Ctlgrs2068824
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23936387OA-icon.png]
Trait Celiac disease
Title A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele C
P-val 6E-6
Odds Ratio NR NR