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: rs10036386
rs10036386
2 1.000 0.040 5 77247778 intron variant C/T snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs1382879
rs1382879
3 1.000 0.040 5 77226043 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1479567
rs1479567
2 1.000 0.040 5 77232197 intron variant G/A;C snv 0.700 1.000 1 2016 2016