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: rs1006207
rs1006207
1 11 64082340 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1212642
rs1212642
1 11 64077822 intron variant A/G snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs139612658
rs139612658
1 11 64125482 intron variant C/T snv 5.4E-04 0.700 1.000 1 2018 2018
dbSNP: rs1807304
rs1807304
1 11 64092279 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018