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: rs10928240
rs10928240
1 2 145062903 intron variant C/G snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs786244
rs786244
1 2 144998693 intron variant C/G snv 0.70 0.700 1.000 1 2019 2019