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: rs10165970
rs10165970
18 0.708 0.320 2 100840527 intron variant G/A snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs1369481
rs1369481
2 0.925 0.080 2 100895497 intron variant T/C snv 0.77 0.010 1.000 1 2009 2009
dbSNP: rs17024869
rs17024869
18 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 0.010 1.000 1 2017 2017
dbSNP: rs17024926
rs17024926
4 0.851 0.120 2 100889540 intron variant T/C snv 0.34 0.010 1.000 1 2009 2009
dbSNP: rs6542993
rs6542993
2 0.925 0.080 2 100824202 intron variant T/A snv 0.33 0.010 1.000 1 2019 2019
dbSNP: rs7581886
rs7581886
18 0.708 0.320 2 100964784 intron variant C/T snv 0.92 0.010 1.000 1 2017 2017
dbSNP: rs895520
rs895520
23 0.689 0.320 2 100961475 intron variant G/A snv 0.35 0.010 1.000 1 2017 2017
dbSNP: rs895521
rs895521
2 0.925 0.080 2 100935633 intron variant T/C snv 0.84 0.010 1.000 1 2009 2009