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: rs17814604
rs17814604 		1 6 98137626 intron variant A/G snv 0.19 0.700 1.000 4 2017 2019
dbSNP: rs2251499
rs2251499 		2 1.000 0.040 13 105987507 intron variant T/A;C;G snv 0.700 1.000 4 2017 2019
dbSNP: rs6801153
rs6801153 		2 1.000 0.040 3 24072206 intergenic variant T/C snv 0.74 0.700 1.000 4 2017 2019
dbSNP: rs9384679
rs9384679 		1 6 108543216 intron variant C/T snv 0.46 0.700 1.000 4 2017 2019
dbSNP: rs10149470
rs10149470 		3 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 0.700 1.000 3 2017 2019
dbSNP: rs10733389
rs10733389 		1 9 23378222 intron variant A/C;G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs11793831
rs11793831 		2 9 23362313 intron variant G/A;T snv 0.700 1.000 3 2018 2019
dbSNP: rs12025777
rs12025777 		1 1 41283225 intron variant G/T snv 8.3E-02 0.700 1.000 3 2018 2019
dbSNP: rs12206087
rs12206087 		2 1.000 0.040 6 98135024 intron variant G/A snv 0.39 0.700 1.000 3 2017 2019
dbSNP: rs12744310
rs12744310 		1 1 41307830 intron variant C/T snv 0.18 0.700 1.000 3 2017 2019
dbSNP: rs13425585
rs13425585 		1 2 156630761 intergenic variant C/G snv 0.51 0.700 1.000 3 2017 2019
dbSNP: rs1933720
rs1933720 		1 6 97849956 intron variant T/C snv 0.26 0.700 1.000 3 2018 2019
dbSNP: rs2426132
rs2426132 		1 20 49106590 intergenic variant G/C snv 0.47 0.700 1.000 3 2017 2019
dbSNP: rs4587178
rs4587178 		1 6 97974115 intron variant T/C snv 0.43 0.700 1.000 3 2018 2019
dbSNP: rs4851300
rs4851300 		1 2 100342342 intergenic variant C/A;T snv 0.700 1.000 3 2018 2019
dbSNP: rs6568547
rs6568547 		1 6 108535175 intron variant C/T snv 0.24 0.700 1.000 3 2018 2019
dbSNP: rs6931604
rs6931604 		1 6 98130339 intron variant C/T snv 0.52 0.700 1.000 3 2018 2019
dbSNP: rs7646501
rs7646501 		1 3 24037800 intergenic variant A/G snv 0.41 0.700 1.000 3 2017 2019
dbSNP: rs77418166
rs77418166 		1 6 97756622 intron variant C/T snv 6.8E-02 0.700 1.000 3 2017 2018
dbSNP: rs942353
rs942353 		1 13 105979225 intron variant C/T snv 0.36 0.700 1.000 3 2018 2019
dbSNP: rs10192369
rs10192369 		2 2 160524377 intergenic variant G/A snv 0.45 0.700 1.000 2 2018 2019
dbSNP: rs10757416
rs10757416 		1 9 23344739 intron variant C/T snv 0.35 0.700 1.000 2 2018 2019
dbSNP: rs10757417
rs10757417 		2 1.000 0.040 9 23347855 intron variant G/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs1106761
rs1106761 		2 8 141609134 intron variant G/A snv 0.28 0.700 1.000 2 2018 2019
dbSNP: rs11153822
rs11153822 		1 6 97766938 intron variant C/T snv 0.40 0.700 1.000 2 2018 2018