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: rs13361707
rs13361707
7 0.882 0.120 5 40791782 intron variant C/T snv 0.31 0.780 1.000 11 2011 2018
dbSNP: rs10074991
rs10074991
7 0.851 0.120 5 40790449 intron variant G/A snv 0.31 0.720 1.000 3 2014 2018
dbSNP: rs154268
rs154268
3 0.925 0.080 5 40795766 intron variant C/T snv 0.69 0.020 1.000 2 2014 2018
dbSNP: rs6882903
rs6882903
2 0.925 0.080 5 40765760 intron variant A/C snv 2.7E-03 0.020 1.000 2 2014 2018
dbSNP: rs3805490
rs3805490
2 0.925 0.080 5 40792051 intron variant T/A snv 0.21 0.010 1.000 1 2018 2018
dbSNP: rs461404
rs461404
3 0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 0.010 1.000 1 2018 2018