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: rs10510388
rs10510388
1 3 8215887 intron variant A/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs17048879
rs17048879
1 3 8233854 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs6777332
rs6777332
1 3 8182251 intron variant C/G;T snv 0.700 1.000 1 2018 2018