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: rs10760442
rs10760442
2 1.000 0.040 9 126621621 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs62578127
rs62578127
1 1.000 0.040 9 126624581 intron variant C/G;T snv 0.700 1.000 1 2019 2019