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: rs6449213
rs6449213
SLC2A9 ; LOC105374476
7 0.827 0.240 4 9992591 intron variant C/T snv 0.82 0.700 0
dbSNP: rs737267
rs737267
SLC2A9
7 0.851 0.240 4 9933120 intron variant G/A;T snv 0.700 0
dbSNP: rs7442295
rs7442295
SLC2A9
5 0.925 0.120 4 9964756 intron variant A/G snv 0.28 0.700 0