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rs348601

From SNPedia

Orientationminus
Stabilizedminus
Make rs348601(A;A)
Make rs348601(A;G)
Make rs348601(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position40319904
is asnp
is mentioned by
dbSNPrs348601
ebirs348601
HLIrs348601
Exacrs348601
Varsomers348601
Maprs348601
PheGenIrs348601
hapmaprs348601
1000 genomesrs348601
hgdprs348601
ensemblrs348601
gopubmedrs348601
geneviewrs348601
scholarrs348601
googlers348601
pharmgkbrs348601
gwascentralrs348601
openSNPrs348601
23andMers348601
23andMe allrs348601
SNP Nexus

SNPshotrs348601
SNPdbers348601
MSV3drs348601
GWAS Ctlgrs348601
GMAF0.477
Max Magnitude
? (A;A) (A;G) (G;G) 28

rs348601 increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele [PMID 17447842OA-icon.png]