Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 Biomarker disease BEFREE Vitiligo was significantly associated with single-nucleotide polymorphisms (SNPs) in a 30-kb LD block on chromosome 6q27, in close vicinity to IDDM8, a linkage and association signal for type I diabetes mellitus and rheumatoid arthritis. 19890347 2010
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 GeneticVariation disease BEFREE The IDDM8 region on chromosome 6q27, first identified as a susceptibility locus for type 1 diabetes, has previously been linked and associated with rheumatoid arthritis (RA). 16945141 2006
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 Biomarker disease BEFREE These findings suggest that the PDCD2 gene is a likely susceptibility gene for T1D within IDDM8. 15848047 2005
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 GeneticVariation disease BEFREE A microsatellite marker allele and multiple haplotypes were associated with IDDM8, which suggests localization of this type 1 diabetes susceptibility gene to the terminal 200 kb of chromosome 6. 10868976 2000
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 Biomarker disease BEFREE We could not confirm linkage for IDDM5, IDDM8 and IDDM15 in our population, possibly due to population-specific differences in genetic susceptibility and/or environmental triggering factors to type 1 diabetes. 11204251 2000
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 GeneticVariation disease BEFREE We developed a statistical method to test this hypothesis in a panel of 523 multiplex families from France, the United States, and Denmark (a total of 667 affected sib pairs, 536 with both parents genotyped), and here present evidence (P = .00003) of a susceptibility locus for IDDM located 32 cM from HLA in males but not linked to HLA in females and distinct from IDDM5 and IDDM8. 8981961 1997
Entrez Id: 3407
Gene Symbol: IDDM8
IDDM8
0.070 GeneticVariation disease BEFREE Linkage analysis of type 1 diabetes sib pair families (n = 334) has suggested two separate regions of human chromosome 6q are linked to disease (designated IDDM5 and IDDM8). 8817350 1996