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: rs12513481
rs12513481
3 5 78155004 intron variant G/C snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs252746
rs252746
2 5 78096293 intron variant A/G snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs425102
rs425102
2 5 78100576 intron variant T/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs72776440
rs72776440
2 5 78144372 intron variant G/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs72776472
rs72776472
1 5 78199207 intron variant A/G snv 0.19 0.700 1.000 1 2019 2019