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: rs141237278
rs141237278 		2 11 47899441 regulatory region variant G/T snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs142286129
rs142286129 		1 11 54688761 upstream gene variant T/C snv 7.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs1423386
rs1423386 		1 5 62689026 intergenic variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs143860577
rs143860577 		1 11 50513762 intergenic variant A/T snv 7.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs144405847
rs144405847 		1 1 82342193 intron variant C/T snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs147455989
rs147455989 		1 11 50161397 intergenic variant T/C snv 7.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs148268781
rs148268781 		1 11 50663948 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs149903077
rs149903077 		1 11 46328146 upstream gene variant G/T snv 9.5E-03 0.700 1.000 1 2019 2019
dbSNP: rs181813804
rs181813804 		1 11 48706704 intergenic variant A/G snv 8.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs182484222
rs182484222 		1 11 48190205 intergenic variant G/A snv 7.7E-03 0.700 1.000 1 2019 2019
dbSNP: rs182879407
rs182879407 		1 11 47199227 intergenic variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs189484085
rs189484085 		1 11 48511937 upstream gene variant C/T snv 8.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs190666382
rs190666382 		1 11 54553509 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1910358
rs1910358 		1 5 23907464 intergenic variant C/T snv 0.72 0.700 1.000 1 2013 2013
dbSNP: rs191436110
rs191436110 		1 1 170621629 intron variant A/G snv 3.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs192463896
rs192463896 		1 11 49093547 downstream gene variant C/G snv 7.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs192874339
rs192874339 		1 11 49397227 intergenic variant A/G snv 7.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs1985317
rs1985317 		1 9 117530056 intergenic variant C/T snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs2028385
rs2028385 		1 12 96423644 intron variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs2144940
rs2144940 		1 20 23070169 downstream gene variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2567617
rs2567617 		1 20 23068910 downstream gene variant G/A snv 0.88 0.010 1.000 1 2016 2016
dbSNP: rs2748331
rs2748331 		1 6 71011625 regulatory region variant T/C snv 0.36 0.010 1.000 1 2017 2017
dbSNP: rs2771051
rs2771051 		1 9 117525430 intergenic variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs28496996
rs28496996 		1 18 1952126 intron variant T/G snv 3.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs28802027
rs28802027 		1 X 155390840 intergenic variant G/T snv 0.11 0.700 1.000 1 2019 2019