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rs1373692

From SNPedia

Orientationminus
Stabilizedminus
Make rs1373692(G;G)
Make rs1373692(G;T)
Make rs1373692(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position40431081
is asnp
is mentioned by
dbSNPrs1373692
ebirs1373692
HLIrs1373692
Exacrs1373692
Varsomers1373692
Maprs1373692
PheGenIrs1373692
hapmaprs1373692
1000 genomesrs1373692
hgdprs1373692
ensemblrs1373692
gopubmedrs1373692
geneviewrs1373692
scholarrs1373692
googlers1373692
pharmgkbrs1373692
gwascentralrs1373692
openSNPrs1373692
23andMers1373692
23andMe allrs1373692
SNP Nexus

SNPshotrs1373692
SNPdbers1373692
MSV3drs1373692
GWAS Ctlgrs1373692
GMAF0.4761
Max Magnitude
? (G;G) (G;T) (T;T) 28

rs1373692 increases susceptibility to Crohn's disease 1.46 times for carriers of the G allele [PMID 17447842OA-icon.png]

GWAS
SNP rs1373692
PubMedID [PMID 17447842OA-icon.png]
Condition Crohn's disease
Gene Intergenic
Risk Allele
pValue 2.00E-012
OR 1.46
95% CI


OMIM612262
DescINFLAMMATORY BOWEL DISEASE 18; IBD18
Variant
Relatedalso



GET Evidence
rs1373692
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.578125
summary