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: rs6687487
rs6687487
1 1 22735058 intron variant G/A snv 8.2E-02 0.700 1.000 2 2018 2018
dbSNP: rs144045260
rs144045260
1 1 22728227 intron variant GAAT/-;GAATGAAT delins 8.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs2043970
rs2043970
1 1 22735465 intron variant A/C snv 8.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs28455953
rs28455953
1 1 22734458 intron variant A/G;T snv 8.5E-02 0.700 1.000 1 2018 2018