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: rs12914623
rs12914623
1 15 80701229 intron variant G/C snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs2759315
rs2759315
1 15 80717305 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs34769775
rs34769775
1 15 80696831 intron variant C/T snv 0.30 0.700 1.000 1 2019 2019