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: rs10738186
rs10738186
1 9 10753414 intergenic variant G/A snv 0.80 0.700 1.000 1 2018 2018
dbSNP: rs10799590
rs10799590
2 1 224634780 intron variant G/A snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10995853
rs10995853
1 10 64259979 intron variant C/G snv 3.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11163319
rs11163319
1 1 81506757 intron variant A/C snv 9.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs12104412
rs12104412
2 1.000 0.080 19 36240156 intron variant A/G;T snv 4.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs12442183
rs12442183
2 1.000 0.080 15 93204756 intergenic variant C/T snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs13097862
rs13097862
1 3 63733563 intergenic variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13279512
rs13279512
1 8 61045943 intergenic variant G/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs1557219
rs1557219
1 6 58044647 intron variant C/T snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs17300532
rs17300532
1 5 72084528 downstream gene variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs1772578
rs1772578
2 1.000 0.080 13 80614113 downstream gene variant A/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs1872052
rs1872052
1 15 93209649 intergenic variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs192590503
rs192590503
1 6 124215869 intron variant G/A snv 2.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs1970606
rs1970606
1 6 58042294 intron variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs4300379
rs4300379
1 11 54614287 intergenic variant C/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs58356853
rs58356853
1 10 122011617 intron variant C/T snv 9.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs59675243
rs59675243
1 10 122011107 intron variant C/A snv 9.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs73568641
rs73568641
2 1.000 0.080 6 153704004 intergenic variant T/C snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs74641711
rs74641711
1 18 79727394 intron variant C/T snv 1.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs75449825
rs75449825
1 10 122010374 intron variant C/A;G snv 9.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs7578347
rs7578347
2 1.000 0.080 2 12981042 non coding transcript exon variant C/T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs8036747
rs8036747
1 15 93209226 intergenic variant G/A snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs9360217
rs9360217
2 1.000 0.080 6 66628700 intergenic variant T/G snv 0.21 0.700 1.000 1 2017 2017