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rs6691768

From SNPedia

Orientationplus
Stabilizedplus
Make rs6691768(A;A)
Make rs6691768(A;G)
Make rs6691768(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position61326191
GeneNFIA
is asnp
is mentioned by
dbSNPrs6691768
ebirs6691768
HLIrs6691768
Exacrs6691768
Varsomers6691768
Maprs6691768
PheGenIrs6691768
hapmaprs6691768
1000 genomesrs6691768
hgdprs6691768
ensemblrs6691768
gopubmedrs6691768
geneviewrs6691768
scholarrs6691768
googlers6691768
pharmgkbrs6691768
gwascentralrs6691768
openSNPrs6691768
23andMers6691768
23andMe allrs6691768
SNP Nexus

SNPshotrs6691768
SNPdbers6691768
MSV3drs6691768
GWAS Ctlgrs6691768
GMAF0.4624
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 1E-7
Odds Ratio 1.11 [1.06-1.15]