Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1058026
rs1058026
5 0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 0.700 1.000 1 2007 2007
dbSNP: rs1634747
rs1634747
1 1.000 0.120 6 31314099 intron variant G/A snv 0.41 0.700 1.000 1 2007 2007
dbSNP: rs2156875
rs2156875
6 0.882 0.200 6 31349570 intron variant C/T snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs2247056
rs2247056
8 0.882 0.160 6 31297713 intron variant T/C snv 0.80 0.700 1.000 1 2007 2007
dbSNP: rs2249742
rs2249742
5 0.925 0.120 6 31272944 intron variant C/T snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs2395471
rs2395471
5 0.925 0.120 6 31272915 intron variant G/A snv 0.47 0.700 1.000 1 2007 2007
dbSNP: rs2442719
rs2442719
1 0.882 0.120 6 31352761 intron variant C/T snv 0.53 0.700 1.000 1 2007 2007
dbSNP: rs2596501
rs2596501
3 0.882 0.200 6 31353434 intron variant C/T snv 0.57 0.700 1.000 1 2007 2007
dbSNP: rs3094682
rs3094682
1 1.000 0.120 6 31296684 intron variant A/C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs3094691
rs3094691
1 1.000 0.120 6 31306916 intron variant G/A snv 0.51 0.700 1.000 1 2007 2007
dbSNP: rs3132486
rs3132486
2 0.925 0.160 6 31275393 intron variant G/A snv 0.49 0.700 1.000 1 2007 2007
dbSNP: rs3134792
rs3134792
3 0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 0.700 1.000 1 2007 2007
dbSNP: rs4386816
rs4386816
5 0.925 0.120 6 31279358 intron variant T/C snv 0.17 0.700 1.000 1 2007 2007
dbSNP: rs6457374
rs6457374
7 0.851 0.200 6 31304484 intron variant C/T snv 0.81 0.700 1.000 1 2007 2007
dbSNP: rs6906846
rs6906846
6 0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 0.700 1.000 1 2007 2007
dbSNP: rs7755852
rs7755852
1 1.000 0.120 6 31310211 intron variant A/G snv 0.49 0.700 1.000 1 2007 2007
dbSNP: rs9265797
rs9265797
1 1.000 0.120 6 31340853 intron variant G/A snv 0.30 0.700 1.000 1 2007 2007