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: rs7041847
rs7041847
1 1.000 0.080 9 4287466 intron variant A/G snv 0.37 0.820 1.000 2 2011 2019
dbSNP: rs10758593
rs10758593
1 0.827 0.240 9 4292083 intron variant G/A snv 0.45 0.800 1.000 1 2012 2014
dbSNP: rs10814916
rs10814916
2 0.851 0.200 9 4293150 intron variant A/C snv 0.57 0.800 1.000 1 2013 2013
dbSNP: rs7034200
rs7034200
3 1.000 0.080 9 4289050 intron variant C/A;G snv 0.750 1.000 1 2011 2019
dbSNP: rs10974438
rs10974438
3 0.925 0.120 9 4291928 intron variant A/C snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs1017568
rs1017568
1 1.000 0.080 9 3948365 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs4258054
rs4258054
1 1.000 0.080 9 4297892 intron variant T/C snv 0.33 0.700 1.000 1 2016 2016