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: rs756481
rs756481
1 22 32709241 intron variant A/G snv 5.7E-02 0.700 1.000 2 2018 2018
dbSNP: rs5754198
rs5754198
1 22 32666245 intron variant G/T snv 4.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs5754221
rs5754221
1 22 32707469 intron variant T/C snv 6.9E-02 0.700 1.000 1 2018 2018