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: rs143709408
rs143709408
5 0.882 0.200 11 2527999 missense variant C/T snv 1.6E-04 3.6E-04 0.700 1.000 1 2018 2018
dbSNP: rs163160
rs163160
2 11 2768725 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs231889
rs231889
1 11 2755962 intron variant C/T snv 0.86 0.700 1.000 1 2019 2019
dbSNP: rs233438
rs233438
1 11 2773162 intron variant G/A snv 0.84 0.700 1.000 1 2019 2019
dbSNP: rs63934
rs63934
1 11 2767832 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs81205
rs81205
1 11 2777574 intron variant A/C snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs84178
rs84178
2 11 2753144 intron variant A/G snv 0.88 0.700 1.000 1 2017 2017