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: rs10161441
rs10161441
1 12 73136489 intron variant C/T snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs1060604
rs1060604
1 1 156214477 intron variant T/C snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs10785010
rs10785010
1 12 73157487 upstream gene variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs10879561
rs10879561
1 12 73139547 intron variant A/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10879567
rs10879567
1 12 73156312 upstream gene variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs10879568
rs10879568
1 12 73156497 upstream gene variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10879569
rs10879569
1 12 73157101 upstream gene variant A/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10879572
rs10879572
1 12 73157791 upstream gene variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs11179569
rs11179569
1 12 73153274 intergenic variant G/A;C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs11179580
rs11179580
1 12 73192799 intron variant C/T snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs1137703
rs1137703
1 1 156214667 intron variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs11587860
rs11587860
1 1 156187160 downstream gene variant G/C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs11655160
rs11655160
1 17 10989753 intergenic variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs12811378
rs12811378
1 12 73160134 intron variant C/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12813018
rs12813018
1 12 73160218 intron variant T/A snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12826112
rs12826112
1 12 73162120 intron variant T/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs1516058
rs1516058
1 12 73137889 intron variant T/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs1606958
rs1606958
1 12 73266151 intergenic variant C/A snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs1976729
rs1976729
1 12 73159309 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs1976730
rs1976730
1 12 73159402 non coding transcript exon variant A/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs2176205
rs2176205
1 12 73159438 non coding transcript exon variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs2241108
rs2241108
1 1 156211216 3 prime UTR variant C/G snv 0.43 0.700 1.000 1 2014 2014
dbSNP: rs2244144
rs2244144
1 1 156214807 intron variant G/A snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs2248074
rs2248074
1 1 156226097 intron variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs2251636
rs2251636
1 1 156233018 intron variant G/C snv 0.41 0.700 1.000 1 2014 2014