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: rs10049390
rs10049390
10 0.776 0.080 3 133982275 intron variant G/A snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs113569514
rs113569514
9 0.790 0.080 3 134029945 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs61510274
rs61510274
9 0.790 0.080 3 134030671 intron variant G/A;C snv 0.700 1.000 1 2018 2018