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: rs6935076
rs6935076
2 0.925 0.120 6 24644094 intron variant C/T snv 0.30 0.020 1.000 2 2016 2018
dbSNP: rs2760157
rs2760157
1 1.000 0.120 6 24578044 intron variant G/A snv 0.28 0.010 < 0.001 1 2014 2014
dbSNP: rs3756821
rs3756821
1 1.000 0.120 6 24646593 upstream gene variant C/T snv 0.42 0.010 1.000 1 2016 2016
dbSNP: rs807507
rs807507
1 1.000 0.120 6 24579639 intron variant G/A;C snv 0.010 < 0.001 1 2014 2014