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: rs3764650
rs3764650
9 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.030 1.000 3 2015 2020
dbSNP: rs4147929
rs4147929
3 0.882 0.120 19 1063444 intron variant A/C;G snv 0.010 1.000 1 2020 2020
dbSNP: rs770510230
rs770510230
1 1.000 0.080 19 1058155 stop gained G/T snv 2.0E-05 4.2E-05 0.010 1.000 1 2015 2015