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: rs6732795
rs6732795
1 2 69184385 intron variant A/C snv 0.51 0.700 1.000 3 2017 2018
dbSNP: rs10173269
rs10173269
1 2 69180588 intron variant T/G snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs6546486
rs6546486
1 2 69186760 intron variant A/T snv 0.42 0.700 1.000 1 2018 2018