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: 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: rs10022499
rs10022499
SLC2A9 ; LOC105374476
3 0.925 0.120 4 10004913 intron variant C/A snv 0.72 0.700 1.000 3 2010 2013
dbSNP: rs10023068
rs10023068
SLC2A9 ; LOC105374476
3 0.925 0.120 4 10003208 intron variant A/G snv 0.72 0.700 1.000 3 2010 2013
dbSNP: rs10033612
rs10033612
SLC2A9
3 0.925 0.120 4 9983382 intron variant C/T snv 0.20 0.700 1.000 3 2010 2013
dbSNP: rs10516200
rs10516200
WDR1 ; MIR3138
3 0.925 0.120 4 10080532 intron variant C/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs10516201
rs10516201 		3 0.925 0.120 4 10122317 intergenic variant T/C snv 0.18 0.700 1.000 3 2010 2013
dbSNP: rs1071988
rs1071988
SLC2A9
3 0.925 0.120 4 9973014 intron variant A/G;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1079128
rs1079128
SLC2A9
3 0.925 0.120 4 9949597 intron variant T/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10792443
rs10792443
NRXN2
2 0.925 0.120 11 64627780 intron variant G/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10805346
rs10805346
SLC2A9
3 0.925 0.120 4 9918723 intron variant T/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10897526
rs10897526
MAP4K2
2 0.925 0.120 11 64792426 splice region variant T/C snv 0.37 0.30 0.700 1.000 3 2010 2013
dbSNP: rs10939650
rs10939650
SLC2A9 ; LOC105374476
3 0.925 0.120 4 9996816 synonymous variant C/G;T snv 1.2E-05; 0.70 0.700 1.000 3 2010 2013
dbSNP: rs10939665
rs10939665
SLC2A9
3 0.925 0.120 4 10036004 non coding transcript exon variant T/C snv 0.43 0.700 1.000 3 2010 2013
dbSNP: rs10939669
rs10939669
SLC2A9
3 0.925 0.120 4 10044203 intron variant A/G;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1109472
rs1109472 		3 0.925 0.120 4 10132824 intergenic variant G/A;C;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1122141
rs1122141
SLC2A9
3 0.925 0.120 4 9945654 intron variant T/C snv 0.57 0.700 1.000 3 2010 2013
dbSNP: rs11231845
rs11231845
NRXN2
2 0.925 0.120 11 64639947 intron variant G/A snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs115810
rs115810
TRIM38
5 0.925 0.120 6 25975655 intron variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs1165148
rs1165148
SLC17A3
3 0.925 0.120 6 25844482 intron variant G/T snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165158
rs1165158
SLC17A3
3 0.925 0.120 6 25864670 intron variant C/A snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165159
rs1165159
SLC17A3
3 0.925 0.120 6 25864397 intron variant A/G snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165161
rs1165161
SLC17A3
3 0.925 0.120 6 25864134 intron variant C/T snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165162
rs1165162
SLC17A3
3 0.925 0.120 6 25863377 intron variant C/T snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165164
rs1165164
SLC17A3
3 0.925 0.120 6 25863253 intron variant G/A snv 0.24 0.700 1.000 3 2010 2013
dbSNP: rs1165165
rs1165165
SLC17A3
3 0.925 0.120 6 25862238 missense variant C/T snv 0.21 0.24 0.700 1.000 3 2010 2013