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: rs12639833
rs12639833
3 1.000 0.080 4 99346215 intron variant C/T snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs1612735
rs1612735
3 1.000 0.080 4 99336850 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1614972
rs1614972
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.700 1.000 1 2014 2014
dbSNP: rs1789924
rs1789924
5 0.925 0.160 4 99353129 upstream gene variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2241894
rs2241894
3 1.000 0.080 4 99344976 synonymous variant T/A;C snv 4.0E-06; 0.30 0.700 1.000 1 2014 2014