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: rs6782812
rs6782812
1 3 128599154 intergenic variant G/A snv 0.89 0.700 1.000 3 2016 2018
dbSNP: rs163574
rs163574
1 3 3055243 intron variant A/G snv 0.88 0.700 1.000 2 2016 2018
dbSNP: rs16823866
rs16823866
1 2 144567410 intron variant T/C snv 0.14 0.700 1.000 2 2016 2018
dbSNP: rs10100356
rs10100356
1 8 129613918 intron variant G/A snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs10401672
rs10401672
1 19 33269055 regulatory region variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs113721499
rs113721499
1 6 31261530 intergenic variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs11579220
rs11579220
1 1 205175235 intron variant G/T snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs11772895
rs11772895
ZYX
1 7 143384849 intron variant G/C snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs11857230
rs11857230
1 15 50100624 intron variant A/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1186222
rs1186222
1 7 75618011 intron variant C/T snv 0.49 0.700 1.000 1 2016 2016
dbSNP: rs1205896
rs1205896
1 6 22341240 intron variant G/A snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs12208785
rs12208785
1 6 109381824 non coding transcript exon variant A/G snv 4.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12445547
rs12445547
1 16 88452161 upstream gene variant G/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs12447180
rs12447180
1 16 88451314 upstream gene variant T/C snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs12762973
rs12762973
1 10 914821 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1292061
rs1292061
1 17 59833869 intron variant A/G snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs144670711
rs144670711
1 2 218037604 intron variant T/C snv 5.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs1474920
rs1474920
1 14 23118346 intron variant G/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs150498232
rs150498232
1 21 35420326 intron variant A/G snv 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs150876292
rs150876292
1 11 69874913 regulatory region variant T/C snv 5.1E-04 0.700 1.000 1 2018 2018
dbSNP: rs1537061
rs1537061
1 1 87273536 regulatory region variant T/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs1669340
rs1669340
1 3 3156696 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1691799
rs1691799
1 12 66327321 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs171835
rs171835
1 6 81755270 upstream gene variant G/A snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs200830364
rs200830364
1 11 90199744 downstream gene variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA delins 0.38 0.700 1.000 1 2016 2016