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rs1032355

From SNPedia

Orientationminus
Stabilizedminus
Make rs1032355(A;A)
Make rs1032355(A;G)
Make rs1032355(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position99618739
GeneMTTP
is asnp
is mentioned by
dbSNPrs1032355
ebirs1032355
HLIrs1032355
Exacrs1032355
Varsomers1032355
Maprs1032355
PheGenIrs1032355
hapmaprs1032355
1000 genomesrs1032355
hgdprs1032355
ensemblrs1032355
gopubmedrs1032355
geneviewrs1032355
scholarrs1032355
googlers1032355
pharmgkbrs1032355
gwascentralrs1032355
openSNPrs1032355
23andMers1032355
23andMe allrs1032355
SNP Nexus

SNPshotrs1032355
SNPdbers1032355
MSV3drs1032355
GWAS Ctlgrs1032355
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 5E-6
Odds Ratio NR NR