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: rs10198275
rs10198275
1 2 24907673 intron variant A/C snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs13035244
rs13035244
1 2 24911140 intron variant T/C snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs55701159
rs55701159
1 2 24916727 intron variant T/G snv 0.11 0.700 1.000 1 2017 2017