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: rs10058621
rs10058621
1 5 51259335 intergenic variant T/C snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs11074779
rs11074779
1 16 26440122 intergenic variant T/C snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs11177782
rs11177782
1 12 69662005 intron variant C/T snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs111882035
rs111882035
1 4 85495401 intron variant A/G snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs112108866
rs112108866
1 19 38761240 intron variant C/A;G snv 1.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs113338984
rs113338984
1 16 69282015 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs116330320
rs116330320
1 4 188507189 intron variant G/A;T snv 3.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs117609474
rs117609474
1 14 53804550 intron variant A/G snv 1.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs11775026
rs11775026
1 8 73264813 intergenic variant T/C snv 5.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs118130881
rs118130881
1 8 31371254 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs12268753
rs12268753
1 10 52058389 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12295181
rs12295181
1 11 5270506 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs12436690
rs12436690
1 14 97119552 intron variant G/A snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs12990252
rs12990252
1 2 35861457 intergenic variant G/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs13053731
rs13053731
1 22 36286661 intron variant G/A snv 5.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs13166268
rs13166268
1 5 121024223 intergenic variant C/G snv 9.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs13360092
rs13360092
1 5 51233341 intergenic variant G/A snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs139139710
rs139139710
1 7 71678504 intron variant C/A snv 2.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs140454225
rs140454225
1 16 1003856 upstream gene variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs142614863
rs142614863
1 5 65950288 intron variant C/T snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs143985312
rs143985312
1 2 77072001 intron variant T/C snv 9.4E-03 0.700 1.000 1 2018 2018
dbSNP: rs1449587
rs1449587
1 13 48839332 regulatory region variant C/T snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs145471199
rs145471199
1 7 9407441 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs147828834
rs147828834
1 15 39602982 intron variant A/T snv 8.3E-03 0.700 1.000 1 2018 2018
dbSNP: rs148410317
rs148410317
1 11 1749985 intron variant G/A;C snv 0.700 1.000 1 2018 2018