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: rs84178
rs84178
2 11 2753144 intron variant A/G snv 0.88 0.700 1.000 1 2017 2017