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: rs10015639
rs10015639
1 4 86970413 intron variant A/G snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs10023020
rs10023020
1 4 121803449 intron variant G/A snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10023050
rs10023050
1 4 87143279 downstream gene variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs10023056
rs10023056
1 4 87143314 downstream gene variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs10032244
rs10032244
1 4 86996779 intron variant A/G snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs1003688
rs1003688
2 6 25658944 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1006081
rs1006081
1 6 109304347 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1007176
rs1007176
1 6 164070805 intergenic variant A/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs1008084
rs1008084
3 6 109305762 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs10080880
rs10080880
1 6 134868890 intergenic variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10084948
rs10084948
1 4 121844494 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10086987
rs10086987
2 1.000 0.040 8 47177908 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1009082
rs1009082
1 17 20159646 intron variant G/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs10099197
rs10099197
1 8 41796940 intron variant C/T snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs1010222
rs1010222
3 19 12937794 upstream gene variant A/G snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs1010549
rs1010549
1 6 164071351 intergenic variant A/C snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs1010902
rs1010902
1 4 86898002 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1010903
rs1010903
1 4 86898040 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10109400
rs10109400
1 8 42600210 intergenic variant T/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs1012898
rs1012898
1 6 25604487 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs1013891
rs1013891
1 6 135217501 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1014021
rs1014021
1 6 135013462 intron variant A/G snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs1015149
rs1015149
1 6 41691151 synonymous variant C/T snv 0.46 0.50 0.700 1.000 1 2012 2012
dbSNP: rs1015150
rs1015150
1 6 41691566 intron variant C/T snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs1015670
rs1015670
1 19 2171491 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012