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: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs1333047
rs1333047
9 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
dbSNP: rs4380028
rs4380028
7 0.807 0.120 15 78818751 intron variant C/T snv 0.34 0.010 1.000 1 2017 2017
dbSNP: rs4731702
rs4731702
5 0.925 0.120 7 130748625 intergenic variant C/T snv 0.40 0.010 1.000 1 2012 2012