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: rs10437954
rs10437954
1 12 57610139 upstream gene variant G/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs2014912
rs2014912
1 4 85794517 intron variant T/C snv 0.84 0.700 1.000 3 2015 2017
dbSNP: rs57400569
rs57400569
1 4 88831125 intron variant G/A snv 0.22 0.700 1.000 3 2017 2019
dbSNP: rs10048404
rs10048404
1 18 56911251 intron variant C/T snv 0.28 0.700 1.000 2 2018 2019
dbSNP: rs1012089
rs1012089
1 16 74138074 intron variant C/G;T snv 0.40 0.700 1.000 2 2018 2019
dbSNP: rs10852858
rs10852858
CRK
1 17 1454457 intron variant C/T snv 0.39 0.700 1.000 2 2019 2019
dbSNP: rs11112548
rs11112548
1 12 105478136 regulatory region variant A/T snv 3.3E-02 0.700 1.000 2 2018 2019
dbSNP: rs11210029
rs11210029
1 1 41399621 regulatory region variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs112184198
rs112184198
1 10 100844757 intergenic variant G/A snv 9.3E-02 0.700 1.000 2 2017 2019
dbSNP: rs11632436
rs11632436
1 15 85752055 intron variant G/A;C snv 0.39 0.700 1.000 2 2018 2019
dbSNP: rs11876341
rs11876341
1 18 51273621 regulatory region variant A/G snv 0.23 0.700 1.000 2 2018 2019
dbSNP: rs12035750
rs12035750
1 1 88866416 intron variant T/C snv 0.27 0.700 1.000 2 2019 2019
dbSNP: rs12050260
rs12050260
1 14 23291885 intron variant T/C snv 0.56 0.700 1.000 2 2017 2019
dbSNP: rs12153395
rs12153395
1 5 179984477 intron variant G/A;T snv 7.2E-02 0.700 1.000 2 2018 2019
dbSNP: rs12705390
rs12705390
1 7 106770331 upstream gene variant G/A snv 0.17 0.700 1.000 2 2016 2019
dbSNP: rs1331012
rs1331012
1 13 26541287 intergenic variant G/T snv 0.21 0.700 1.000 2 2018 2019
dbSNP: rs1764975
rs1764975
1 20 4120643 upstream gene variant T/A snv 0.85 0.700 1.000 2 2018 2019
dbSNP: rs189267552
rs189267552
1 3 20031701 intergenic variant T/A snv 8.8E-03 0.700 1.000 2 2018 2019
dbSNP: rs1898165
rs1898165
1 18 75328421 intergenic variant G/A;C snv 0.700 1.000 2 2019 2019
dbSNP: rs2012714
rs2012714
1 22 19990124 intron variant C/T snv 0.34 0.700 1.000 2 2017 2018
dbSNP: rs2188717
rs2188717
1 16 24718909 intron variant T/A;C snv 0.700 1.000 2 2019 2019
dbSNP: rs231708
rs231708
1 4 2693046 intron variant G/C;T snv 0.59 0.700 1.000 2 2018 2019
dbSNP: rs2354862
rs2354862
1 8 63589186 non coding transcript exon variant A/C snv 0.25 0.700 1.000 2 2018 2019
dbSNP: rs2613765
rs2613765
1 19 5066319 intron variant G/A snv 0.42 0.700 1.000 2 2018 2019
dbSNP: rs28558491
rs28558491
1 2 186951594 intergenic variant C/T snv 0.62 0.700 1.000 2 2018 2019