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: rs1883025
rs1883025
13 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 5 2009 2013
dbSNP: rs3890182
rs3890182
5 0.925 0.120 9 104885374 intron variant G/A;T snv 0.700 1.000 3 2008 2012
dbSNP: rs12686004
rs12686004
6 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 0.700 1.000 2 2011 2012
dbSNP: rs9282541
rs9282541
13 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 0.700 1.000 2 2008 2013
dbSNP: rs10120087
rs10120087
2 9 104898869 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11789603
rs11789603
3 9 104884738 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs12341993
rs12341993
3 9 104896629 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13284054
rs13284054
3 9 104906792 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs13290420
rs13290420
3 9 104886684 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs2000069
rs2000069
2 9 104873588 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2066714
rs2066714
13 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 0.700 1.000 1 2012 2012
dbSNP: rs2066718
rs2066718
7 0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs2254819
rs2254819
3 9 104904133 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2275544
rs2275544
3 9 104888931 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs2275545
rs2275545
2 9 104889245 intron variant A/G snv 0.14 0.18 0.700 1.000 1 2012 2012
dbSNP: rs2515629
rs2515629
3 1.000 0.040 9 104832083 intron variant A/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs2575876
rs2575876
7 9 104903458 intron variant G/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2777795
rs2777795
4 9 104910084 intron variant G/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs3780543
rs3780543
2 9 104826291 intron variant A/G snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs3847300
rs3847300
3 9 104886149 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs3847305
rs3847305
3 9 104894972 intron variant G/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs3858076
rs3858076
3 9 104893841 intron variant A/C snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs3905000
rs3905000
5 0.925 0.080 9 104894789 intron variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs3905001
rs3905001
2 9 104905783 intron variant G/C snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs4100654
rs4100654
3 9 104906960 intron variant T/C snv 8.3E-02 0.700 1.000 1 2012 2012