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: rs2871865
rs2871865
2 15 98651667 intron variant C/G snv 0.21 0.700 1.000 4 2010 2019
dbSNP: rs10902605
rs10902605
1 15 98667368 intron variant G/C snv 0.91 0.700 1.000 1 2017 2017
dbSNP: rs2684777
rs2684777
1 15 98853465 intron variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs62024476
rs62024476
1 15 98687876 intron variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs8033670
rs8033670
1 15 98955650 intron variant T/A;C snv 0.700 1.000 1 2019 2019