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: rs200085146
rs200085146
1 11 94447287 missense variant C/T snv 2.0E-05 7.0E-06 0.700 0
dbSNP: rs748434421
rs748434421
1 11 94485928 missense variant T/A snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs774057024
rs774057024
1 11 94456331 missense variant C/T snv 1.6E-05 2.8E-05 0.700 0
dbSNP: rs10035650
rs10035650
1 5 94600780 intron variant A/G snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs10138053
rs10138053
1 14 51148434 intergenic variant T/C snv 0.74 0.700 1.000 1 2017 2017
dbSNP: rs10160246
rs10160246
1 11 23153770 upstream gene variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10273639
rs10273639
9 0.776 0.280 7 142749077 upstream gene variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs1029966
rs1029966
1 16 4922962 intron variant C/T snv 0.76 0.700 1.000 1 2017 2017
dbSNP: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs10490913
rs10490913
1 10 118394924 intron variant T/C snv 0.39 0.700 1.000 1 2017 2017
dbSNP: rs10510776
rs10510776
1 3 55162885 downstream gene variant C/A snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs10833965
rs10833965
1 11 23193334 intron variant A/G snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs10854373
rs10854373
1 21 34366284 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11027001
rs11027001
1 11 23133679 intergenic variant T/C snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs11079867
rs11079867
1 17 49277423 intron variant A/C snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs11327
rs11327
1 7 142802725 3 prime UTR variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs11602836
rs11602836
1 11 23211338 intergenic variant C/A;G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11640939
rs11640939
1 16 4982458 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs11641901
rs11641901
1 16 4979496 intron variant A/G snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs11655704
rs11655704
1 17 49370810 non coding transcript exon variant T/C snv 0.11 0.30 0.700 1.000 1 2017 2017
dbSNP: rs11686241
rs11686241
1 2 216433482 intron variant A/G snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs11828289
rs11828289
1 11 23174695 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11861717
rs11861717
PPL
1 16 4941276 intron variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs11864122
rs11864122
1 16 4973520 intron variant C/T snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs11911509
rs11911509
1 21 34469442 intron variant C/A snv 0.700 1.000 1 2017 2017