Source: ALL
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: rs10001106
rs10001106 		3 0.925 0.120 4 10125817 intergenic variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs10001632
rs10001632
CLNK ; LOC105374482
2 0.925 0.120 4 10520247 intron variant A/C snv 0.97 0.700 1.000 1 2013 2013
dbSNP: rs10001964
rs10001964
SLC2A9
3 0.925 0.120 4 9957651 intron variant C/T snv 0.48 0.700 1.000 2 2010 2013
dbSNP: rs10002984
rs10002984 		2 0.925 0.120 4 9679109 intron variant T/C snv 0.95 0.700 1.000 2 2010 2013
dbSNP: rs10003001
rs10003001
SLC2A9
3 0.925 0.120 4 9982851 intron variant C/T snv 0.21 0.700 1.000 3 2010 2013
dbSNP: rs10003864
rs10003864 		3 0.925 0.120 4 10435767 downstream gene variant T/C snv 0.29 0.700 1.000 2 2010 2013
dbSNP: rs10005684
rs10005684 		2 0.925 0.120 4 9625273 intron variant T/A;G snv 0.700 1.000 2 2010 2013
dbSNP: rs10006397
rs10006397
SLC2A9
3 0.925 0.120 4 10034516 non coding transcript exon variant C/A snv 0.78 0.700 1.000 3 2010 2013
dbSNP: rs1000662
rs1000662 		2 0.925 0.120 11 64466347 intergenic variant G/A snv 0.60 0.700 1.000 2 2010 2013
dbSNP: rs10007469
rs10007469 		2 0.925 0.120 4 9731119 upstream gene variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10008035
rs10008035
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9997711 intron variant G/A;T snv 0.700 1.000 2 2010 2013
dbSNP: rs10009493
rs10009493 		3 0.925 0.120 4 10130423 intergenic variant C/G snv 0.18 0.700 1.000 2 2010 2013
dbSNP: rs10009618
rs10009618
ABCG2
3 0.925 0.120 4 88172856 intron variant C/T snv 0.58 0.700 1.000 3 2010 2013
dbSNP: rs10010656
rs10010656 		3 0.925 0.120 4 10244703 intergenic variant G/C snv 0.30 0.700 1.000 2 2010 2013
dbSNP: rs10011206
rs10011206
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9990331 intron variant C/T snv 0.23 0.700 1.000 2 2010 2013
dbSNP: rs10011621
rs10011621 		2 0.925 0.120 4 9758615 downstream gene variant A/C snv 0.22 0.700 1.000 2 2010 2013
dbSNP: rs10011796
rs10011796
ABCG2
4 0.882 0.160 4 88169725 intron variant T/C;G snv 0.800 1.000 4 2010 2015
dbSNP: rs1001216
rs1001216 		3 0.925 0.120 4 10167225 non coding transcript exon variant A/G snv 0.15 0.700 1.000 2 2010 2013
dbSNP: rs1001217
rs1001217 		3 0.925 0.120 4 10167375 non coding transcript exon variant C/A;G snv 0.700 1.000 2 2010 2013
dbSNP: rs10012288
rs10012288 		3 0.925 0.120 4 10139329 downstream gene variant G/A snv 0.42 0.700 1.000 2 2010 2013
dbSNP: rs10012779
rs10012779
SLC2A9
3 0.925 0.120 4 10036488 intron variant C/T snv 0.15 0.700 1.000 2 2010 2013
dbSNP: rs10013288
rs10013288
MIR548I2
2 0.925 0.120 4 9557597 upstream gene variant T/A;G snv 0.700 1.000 2 2010 2013
dbSNP: rs10015494
rs10015494 		3 0.925 0.120 4 10140366 downstream gene variant G/A;C;T snv 0.700 1.000 2 2010 2013
dbSNP: rs10015872
rs10015872 		3 0.925 0.120 4 10140786 downstream gene variant G/A snv 0.42 0.700 1.000 2 2010 2013
dbSNP: rs10016022
rs10016022
ZNF518B
3 0.925 0.120 4 10445282 missense variant A/G;T snv 0.74 0.700 1.000 2 2010 2013