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: rs181509591
rs181509591
SLC2A9 ; LOC105374476
1 1.000 0.160 4 9996817 missense variant G/A;C snv 1.4E-04; 2.4E-05 0.800 1.000 3 2008 2012
dbSNP: rs776127501
rs776127501
SLC2A9
1 1.000 0.160 4 9985693 missense variant G/A snv 3.6E-05 2.1E-05 0.800 1.000 3 2008 2012
dbSNP: rs863225072
rs863225072
SLC2A9
1 1.000 0.160 4 10019000 missense variant A/C snv 6.5E-06 2.8E-05 0.800 1.000 3 2008 2012
dbSNP: rs121908321
rs121908321
SLC2A9
3 0.925 0.200 4 9890687 missense variant G/A;T snv 2.1E-04; 8.0E-06 0.710 1.000 4 2008 2014
dbSNP: rs121908322
rs121908322
SLC2A9
2 1.000 0.160 4 9980681 missense variant G/A snv 3.2E-05 2.1E-05 0.700 1.000 3 2008 2012
dbSNP: rs121908323
rs121908323
SLC2A9
1 1.000 0.160 4 9887623 missense variant G/C snv 5.7E-06 0.700 0
dbSNP: rs763684449
rs763684449
SLC22A12
3 0.925 0.200 11 64600799 missense variant C/A;T snv 9.4E-05 0.010 1.000 1 2014 2014
dbSNP: rs775438172
rs775438172
SLC2A9
1 1.000 0.160 4 9920443 stop gained C/T snv 3.6E-05 2.1E-05 0.010 1.000 1 2019 2019