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: rs1426217
rs1426217
1 1.000 0.040 15 26575978 intron variant A/G snv 0.46 0.010 < 0.001 1 2018 2018
dbSNP: rs2081648
rs2081648
1 1.000 0.040 15 26553052 intron variant T/C snv 0.12 0.010 < 0.001 1 2018 2018
dbSNP: rs25409
rs25409
4 0.882 0.080 15 26773694 missense variant G/A snv 2.9E-03 3.5E-03 0.010 1.000 1 2011 2011