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: 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
dbSNP: rs1165167
rs1165167
SLC17A3
3 0.925 0.120 6 25860460 intron variant A/G snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165187
rs1165187
SLC17A3
3 0.925 0.120 6 25851141 intron variant T/C snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165189
rs1165189
SLC17A3
3 0.925 0.120 6 25849551 intron variant A/C snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs1165205
rs1165205
SLC17A3
4 0.925 0.120 6 25870314 intron variant T/A;G snv 0.700 1.000 3 2008 2013
dbSNP: rs11722228
rs11722228
SLC2A9
6 0.851 0.160 4 9914117 intron variant C/T snv 0.32 0.700 1.000 3 2010 2013
dbSNP: rs11722229
rs11722229
SLC2A9
3 0.925 0.120 4 9979073 intron variant C/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs11722930
rs11722930
SLC2A9
3 0.925 0.120 4 10033830 intron variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs11723439
rs11723439
SLC2A9
3 0.925 0.120 4 9950195 intron variant C/T snv 0.17 0.700 1.000 3 2010 2013
dbSNP: rs11723591
rs11723591
SLC2A9
3 0.925 0.120 4 9983774 intron variant T/A snv 0.42 0.700 1.000 3 2010 2013
dbSNP: rs11723970
rs11723970
SLC2A9
3 0.925 0.120 4 9978838 intron variant T/C snv 0.42 0.700 1.000 3 2010 2013
dbSNP: rs11724510
rs11724510
SLC2A9
3 0.925 0.120 4 9956959 intron variant C/T snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs11727199
rs11727199
SLC2A9
3 0.925 0.120 4 10034566 non coding transcript exon variant C/T snv 0.42 0.700 1.000 3 2010 2013
dbSNP: rs11730059
rs11730059 		4 0.925 0.120 4 87966175 intergenic variant A/G snv 0.93 0.700 1.000 3 2010 2013
dbSNP: rs11731110
rs11731110
SLC2A9
3 0.925 0.120 4 10035722 non coding transcript exon variant T/C snv 0.43 0.700 1.000 3 2010 2013
dbSNP: rs11731597
rs11731597
WDR1
3 0.925 0.120 4 10073861 upstream gene variant C/T snv 0.29 0.700 1.000 3 2010 2013
dbSNP: rs1179087
rs1179087
SLC17A3
3 0.925 0.120 6 25858476 intron variant G/C;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1182814
rs1182814
SLC17A3
3 0.925 0.120 6 25859326 intron variant T/C snv 0.25 0.700 1.000 3 2010 2013
dbSNP: rs11938608
rs11938608 		3 0.925 0.120 4 10134225 intergenic variant T/C snv 0.27 0.700 1.000 3 2010 2013
dbSNP: rs11942223
rs11942223
SLC2A9
4 0.882 0.160 4 9961141 intron variant T/C snv 0.28 0.700 1.000 3 2010 2013
dbSNP: rs12498742
rs12498742
SLC2A9
3 0.925 0.120 4 9942428 intron variant A/G snv 0.33 0.700 1.000 3 2010 2013