Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs202148845 1 173081132 intergenic variant -/A delins 1
rs57476984 15 58426498 intron variant -/A delins 1.4E-05 1
rs113226428 13 107817853 intron variant -/C ins 1
rs57277452 4 2772731 intergenic variant -/C ins 8.1E-04 1
rs61435922 11 41756060 intron variant -/C ins 0.13 1
rs34910943 11 61653517 downstream gene variant -/CTCTG ins 1
rs200666086 10 98397611 intron variant -/CTG delins 1
rs11437675 11 61150558 intron variant -/G ins 3.2E-03 1
rs34766626 11 61144420 non coding transcript exon variant -/G delins 1
rs35088638 16 56962246 5 prime UTR variant -/G delins 1
rs35713313 22 19275329 intron variant -/G delins 1
rs4019045 5 65982680 intron variant -/GACTG ins 0.82 1
rs35328399 4 186217309 intron variant -/GTT delins 1
rs146534688 4 64155298 intergenic variant -/TA;TATACATA delins 1
rs201608675 11 61653518 downstream gene variant -/TCTCTGG;TCTGG ins 0.83 1
rs33930717 4 186257634 intron variant -/TGT;TTT delins 1
rs35826599 22 19269948 intron variant A/-;AA delins 1
rs35253168 6 111199828 intron variant A/-;AA;AAA;AAAA;AAAAA delins 1
rs386408250 6 111199828 intron variant A/-;AA;AAA;AAAA;AAAAA delins 0.22 1
rs174574 1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs7203984 16 56965346 intron variant A/C snv 0.31 7
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 4
rs174536 11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs2602362 2 233607902 downstream gene variant A/C snv 0.22 3