Source: ALL
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: rs11237982
rs11237982 		2 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs117905930
rs117905930 		2 1.000 0.080 9 88973603 intron variant C/A;T snv 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: rs13166268
rs13166268 		1 5 121024223 intergenic variant C/G snv 9.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs140454225
rs140454225 		1 16 1003856 upstream gene variant T/C;G snv 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: rs147906088
rs147906088 		2 1.000 0.080 7 54496119 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs150900094
rs150900094 		1 15 87284961 intergenic variant A/C snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs35551159
rs35551159 		1 12 60075450 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4762194
rs4762194 		1 12 97789941 intergenic variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs4776997
rs4776997 		1 15 67858585 intron variant A/G;T snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs6020113
rs6020113 		1 20 37674643 upstream gene variant G/A snv 9.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs6813517
rs6813517 		1 4 167601600 intergenic variant T/C snv 0.17 0.700 1.000 1 2015 2015
dbSNP: rs74938950
rs74938950 		1 20 12281822 intron variant C/T snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs7557162
rs7557162 		1 2 177057129 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs8073765
rs8073765 		1 17 13726414 regulatory region variant T/C snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs932350
rs932350 		1 1 4793628 downstream gene variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs9528384
rs9528384 		1 13 61728432 regulatory region variant A/G snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs5747035
rs5747035
ADA2
1 22 17237716 intron variant T/C snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs6830160
rs6830160
ANAPC4
1 4 25377604 intron variant G/A;T snv 8.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2015 2015