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: rs821597
rs821597
1 1.000 0.040 1 231966518 intron variant G/A snv 0.49 0.080 0.875 8 2005 2018
dbSNP: rs2053079
rs2053079
1 1.000 0.040 19 30496516 intron variant A/G snv 0.19 0.710 1.000 7 2014 2019
dbSNP: rs11685299
rs11685299
1 1.000 0.040 2 224526579 intron variant C/A snv 0.27 0.700 1.000 6 2014 2019
dbSNP: rs215411
rs215411
1 1.000 0.040 4 23421980 intergenic variant T/A snv 0.33 0.700 1.000 6 2014 2019
dbSNP: rs6490121
rs6490121
1 1.000 0.040 12 117270390 intron variant G/A snv 0.64 0.060 1.000 6 2009 2018
dbSNP: rs12148337
rs12148337
1 1.000 0.040 15 70296933 intergenic variant T/C snv 0.46 0.700 1.000 5 2014 2019
dbSNP: rs12691307
rs12691307
1 1.000 0.040 16 29928556 non coding transcript exon variant A/G snv 0.50 0.710 1.000 5 2014 2019
dbSNP: rs2693698
rs2693698
1 1.000 0.040 14 99252882 intron variant A/G snv 0.59 0.700 1.000 5 2014 2019
dbSNP: rs3918342
rs3918342
1 1.000 0.040 13 105533400 intergenic variant C/T snv 0.46 0.050 1.000 5 2006 2017
dbSNP: rs4240748
rs4240748
1 1.000 0.040 12 91853010 regulatory region variant C/A;G snv 0.700 1.000 5 2014 2019
dbSNP: rs56873913
rs56873913
1 1.000 0.040 19 49587942 intron variant T/G snv 0.33 0.700 1.000 5 2014 2019
dbSNP: rs6002655
rs6002655
1 1.000 0.040 22 42207808 intron variant C/A;T snv 0.700 1.000 5 2014 2019
dbSNP: rs7267348
rs7267348
1 1.000 0.040 20 49514499 intron variant T/C snv 0.29 0.700 1.000 5 2014 2019
dbSNP: rs7523273
rs7523273
1 1.000 0.040 1 207803738 non coding transcript exon variant A/G snv 0.30 0.700 1.000 5 2014 2019
dbSNP: rs778371
rs778371
1 1.000 0.040 2 232878399 non coding transcript exon variant A/G snv 0.27 0.800 1.000 5 2013 2019
dbSNP: rs8082590
rs8082590
1 1.000 0.040 17 18055088 intron variant G/A;T snv 0.700 1.000 5 2014 2019
dbSNP: rs9420
rs9420
1 1.000 0.040 11 57742822 non coding transcript exon variant A/G snv 0.68 0.700 1.000 5 2014 2019
dbSNP: rs10860964
rs10860964
1 1.000 0.040 12 103202677 intergenic variant T/C snv 0.28 0.700 1.000 4 2014 2019
dbSNP: rs11038167
rs11038167
1 1.000 0.040 11 44821583 intron variant A/C;G snv 0.840 0.750 4 2011 2017
dbSNP: rs11693094
rs11693094
1 1.000 0.040 2 184736693 intron variant C/T snv 0.38 0.700 1.000 4 2014 2019
dbSNP: rs1191551
rs1191551
1 1.000 0.040 14 29531199 intergenic variant T/G snv 0.82 0.700 1.000 4 2015 2019
dbSNP: rs1468412
rs1468412
1 1.000 0.040 7 86804135 intron variant A/T snv 0.39 0.040 0.500 4 2003 2014
dbSNP: rs2905426
rs2905426
1 1.000 0.040 19 19367213 regulatory region variant G/T snv 0.49 0.700 1.000 4 2014 2019
dbSNP: rs4330281
rs4330281
1 1.000 0.040 3 17817874 intron variant T/C snv 0.54 0.700 1.000 4 2014 2019
dbSNP: rs4388249
rs4388249
1 1.000 0.040 5 109700365 intron variant C/T snv 0.17 0.700 1.000 4 2014 2019