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: rs12800049
rs12800049
1 11 16227348 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs12801635
rs12801635
1 11 16330999 intron variant T/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs16932777
rs16932777
1 11 16230637 intron variant C/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs35199438
rs35199438
1 11 16609232 intron variant G/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs3809095
rs3809095
1 11 16736699 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs7131442
rs7131442
2 11 16326515 intron variant A/T snv 0.17 0.700 1.000 1 2018 2018