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
7 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 3 2010 2018
dbSNP: rs12686004
rs12686004
3 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 0.800 1.000 1 2012 2018
dbSNP: rs2575876
rs2575876
4 9 104903458 intron variant G/A snv 0.24 0.800 1.000 1 2012 2018
dbSNP: rs10115928
rs10115928
1 9 104888562 intron variant C/T snv 0.47 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: 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: rs2575875
rs2575875
1 9 104900213 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs2777784
rs2777784
1 9 104898778 intron variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs2777795
rs2777795
3 9 104910084 intron variant G/A snv 8.8E-02 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: rs3890182
rs3890182
4 0.925 0.120 9 104885374 intron variant G/A;T snv 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
dbSNP: rs4149268
rs4149268
4 1.000 0.040 9 104884939 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs4149269
rs4149269
3 9 104884840 intron variant A/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs4149272
rs4149272
3 9 104880006 intron variant C/G;T snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs4149273
rs4149273
3 9 104879930 intron variant T/C snv 0.45 0.700 1.000 1 2012 2012