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: rs1965673
rs1965673
1 1.000 0.200 5 168411232 intron variant C/G snv 6.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs2073716
rs2073716
1 1.000 0.200 6 31155220 intron variant C/G snv 6.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs2517411
rs2517411
1 1.000 0.200 6 30992490 downstream gene variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs2848479
rs2848479
1 1.000 0.200 11 98216871 intergenic variant C/T snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs3093953
rs3093953
1 1.000 0.200 6 31506911 intron variant T/G snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs3094584
rs3094584
1 1.000 0.200 6 31416071 intron variant G/A;T snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs3095324
rs3095324
1 1.000 0.200 6 31119356 intron variant C/T snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs386579334
rs386579334
1 1.000 0.200 6 31119356 intron variant C/T snv 0.700 1.000 1 2012 2012
dbSNP: rs4394274
rs4394274
1 1.000 0.200 6 31350387 intron variant C/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs6910516
rs6910516
1 1.000 0.200 6 31376050 non coding transcript exon variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs6933050
rs6933050
5 0.925 0.200 6 31375855 non coding transcript exon variant T/C snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs7775759
rs7775759
6 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs9266490
rs9266490
1 1.000 0.200 6 31372381 intron variant A/G snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs9268861
rs9268861
2 0.925 0.280 6 32462117 intron variant C/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs936551
rs936551
1 1.000 0.200 4 827702 upstream gene variant A/G snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs9368678
rs9368678
1 1.000 0.200 6 31304686 intron variant T/C snv 9.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs9380217
rs9380217
1 1.000 0.200 6 31083776 downstream gene variant C/T snv 6.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1057519328
rs1057519328
1 1.000 0.200 16 3249592 missense variant G/C snv 2.1E-05 0.700 0
dbSNP: rs146597836
rs146597836
1 1.000 0.200 22 17189987 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
dbSNP: rs746055479
rs746055479
1 1.000 0.200 16 50712108 missense variant G/A;T snv 2.4E-05 0.700 0
dbSNP: rs750868279
rs750868279
1 1.000 0.200 22 17203576 missense variant G/A snv 5.2E-05 4.9E-05 0.700 0
dbSNP: rs751454741
rs751454741
1 1.000 0.200 16 3254736 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs752615209
rs752615209
1 1.000 0.200 16 50710956 missense variant C/G;T snv 8.0E-06 0.700 0
dbSNP: rs755659290
rs755659290
1 1.000 0.200 16 3249480 missense variant T/C snv 1.2E-05 1.4E-05 0.700 0
dbSNP: rs774164456
rs774164456
1 1.000 0.200 15 77032888 missense variant G/A;C snv 2.6E-05 0.700 0