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: rs10804493
rs10804493
1 1.000 0.080 3 111835579 intron variant G/A snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs17490701
rs17490701
1 1.000 0.080 3 111869032 intron variant G/A;T snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs73228543
rs73228543
1 1.000 0.080 3 111873991 intron variant G/A snv 0.10 0.700 1.000 1 2018 2018