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: rs1002054
rs1002054
1 14 55062195 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1003645
rs1003645
1 17 36013244 missense variant T/C snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs10083777
rs10083777
2 16 81031677 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs1009647
rs1009647
2 1.000 0.120 14 55413329 upstream gene variant G/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs1009648
rs1009648
1 14 55413451 upstream gene variant T/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1009714
rs1009714
1 14 55512820 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1009977
rs1009977
2 1.000 0.040 14 55136284 intron variant T/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs1009978
rs1009978
1 14 55136343 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10129505
rs10129505
1 14 55309657 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10130783
rs10130783
1 14 55714800 intergenic variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10131232
rs10131232
1 14 54849190 intron variant G/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10131730
rs10131730
1 14 55373374 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10133662
rs10133662
1 14 54849552 intron variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10134019
rs10134019
1 14 55530274 intron variant T/G snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs10134317
rs10134317
1 14 55326730 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134339
rs10134339
1 14 55347662 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10134800
rs10134800
1 14 55168491 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134983
rs10134983
1 14 55168605 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10135789
rs10135789
1 14 54825302 intergenic variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10136596
rs10136596
1 14 55370055 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10137307
rs10137307
1 14 55378467 intron variant T/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10138446
rs10138446
1 14 55412967 upstream gene variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10139354
rs10139354
1 14 55011884 intron variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs10140164
rs10140164
1 14 54939405 3 prime UTR variant A/G snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs10140801
rs10140801
1 14 55263686 intron variant C/T snv 0.55 0.700 1.000 1 2012 2012