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: rs9964939
rs9964939
1 1.000 0.080 18 70260975 intergenic variant G/A snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs995881
rs995881
1 1.000 0.080 5 118588513 intron variant C/G snv 5.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs9942466
rs9942466
1 1.000 0.080 6 158163377 intron variant T/G snv 2.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs991986
rs991986
1 1.000 0.080 11 45445170 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs9907580
rs9907580
1 1.000 0.080 17 33961449 intron variant T/C snv 0.51 0.700 1.000 1 2009 2009
dbSNP: rs9906158
rs9906158
1 1.000 0.080 17 36468752 regulatory region variant T/C snv 6.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs9883185
rs9883185
1 1.000 0.080 3 29696534 intron variant A/G snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs9880149
rs9880149
1 1.000 0.080 3 10644752 intron variant G/A snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs9874888
rs9874888
1 1.000 0.080 3 60030591 intron variant T/A snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs9784858
rs9784858
2 0.925 0.200 6 32819398 intron variant G/C snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs9783018
rs9783018
1 1.000 0.080 1 61669684 regulatory region variant T/C snv 2.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs9679820
rs9679820
1 1.000 0.080 20 55301790 intergenic variant A/G snv 9.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs9674957
rs9674957
1 1.000 0.080 17 71114957 intron variant G/A snv 0.39 0.700 1.000 1 2009 2009
dbSNP: rs9646627
rs9646627
1 1.000 0.080 18 60862720 intron variant A/G snv 1.0E-01 0.700 1.000 1 2009 2009
dbSNP: rs963911
rs963911
1 1.000 0.080 1 91548494 regulatory region variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs962885
rs962885
1 1.000 0.080 17 45858265 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs9626814
rs9626814
1 1.000 0.080 22 46241357 3 prime UTR variant G/A snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs9481463
rs9481463
1 1.000 0.080 6 114645435 intergenic variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs9469240
rs9469240
2 0.925 0.120 6 32722224 downstream gene variant C/T snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs9469220
rs9469220
5 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs9461799
rs9461799
6 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs9373298
rs9373298
1 1.000 0.080 6 141198693 regulatory region variant A/C snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs9368716
rs9368716
4 0.882 0.200 6 32338313 intron variant G/A snv 0.39 0.700 1.000 1 2009 2009
dbSNP: rs9296260
rs9296260
1 1.000 0.080 6 38724661 intron variant C/T snv 0.75 0.700 1.000 1 2009 2009
dbSNP: rs9276440
rs9276440
2 0.925 0.120 6 32747006 3 prime UTR variant A/G;T snv 0.700 1.000 1 2009 2009