Gene: SLC17A2 ×
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: rs1540273
rs1540273
SLC17A2
4 0.925 0.120 6 25923930 intron variant T/C snv 0.42 0.34 0.700 1.000 1 2009 2009
dbSNP: rs1865760
rs1865760
SLC17A2
5 0.925 0.120 6 25916751 synonymous variant C/T snv 0.42 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2071297
rs2071297
SLC17A2
4 0.925 0.120 6 25924285 intron variant G/C snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2071301
rs2071301
SLC17A2
4 0.925 0.120 6 25914035 intron variant C/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3752421
rs3752421
SLC17A2
4 0.925 0.120 6 25918460 intron variant G/A;C snv 0.42; 4.0E-06 0.700 1.000 1 2009 2009
dbSNP: rs3799371
rs3799371
SLC17A2
4 0.925 0.120 6 25912588 downstream gene variant C/T snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3799372
rs3799372
SLC17A2
4 0.925 0.120 6 25922083 intron variant A/G snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3799373
rs3799373
SLC17A2
4 0.925 0.120 6 25928945 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs6932113
rs6932113
SLC17A2
4 0.925 0.120 6 25912870 3 prime UTR variant C/T snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs6938233
rs6938233
SLC17A2
4 0.925 0.120 6 25913849 intron variant C/T snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs9358893
rs9358893
SLC17A2
4 0.925 0.120 6 25921533 intron variant A/G snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs9467636
rs9467636
SLC17A2
4 0.925 0.120 6 25919321 intron variant A/C snv 0.34 0.700 1.000 1 2009 2009