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: rs76428106
rs76428106
10 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 2 2016 2017
dbSNP: rs189992044
rs189992044
2 13 28075859 intron variant C/A snv 3.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs61946325
rs61946325
2 13 28023050 intron variant C/T snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs9551434
rs9551434
2 13 28067434 intron variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs9554228
rs9554228
2 13 28063701 intron variant A/G snv 0.60 0.700 1.000 1 2016 2016