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: rs2278668
rs2278668
1 3 123116385 intron variant T/C snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs920900
rs920900
1 3 123126824 intron variant C/G snv 0.52 0.700 1.000 1 2018 2018