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: rs1801278
rs1801278
29 0.652 0.393 2 226795828 missense variant C/G,T snp 4.0E-06; 5.2E-02 6.0E-02 0.700 12 1992 2004
dbSNP: rs121434581
rs121434581
3 1.000 0.071 17 7285729 missense variant G/A,C snp 4.2E-03; 4.0E-06 3.0E-03 0.700 3 1991 1992
dbSNP: rs104893649
rs104893649
3 1.000 0.071 2 181678529 missense variant C/A snp 0.700 1 1999 1999
dbSNP: rs114202595
rs114202595
4 0.923 0.107 7 127614533 missense variant G/A,T snp 1.2E-04; 9.1E-06 1.3E-04 0.700 1 2001 2001
dbSNP: rs119489103
rs119489103
3 1.000 0.071 11 45898159 missense variant G/A snp 0.700 1 2000 2000
dbSNP: rs121434593
rs121434593
3 1.000 0.071 19 40237979 missense variant C/T snp 0.700 1 2004 2004
dbSNP: rs121913150
rs121913150
3 1.000 0.071 19 7120707 missense variant C/T snp 8.0E-06 0.700 1 1992 1992
dbSNP: rs121918673
rs121918673
4 1.000 0.071 17 37701122 missense variant G/C snp 1.9E-05 0.700 1 2002 2002
dbSNP: rs137853337
rs137853337
3 1.000 0.071 20 44428409 missense variant G/A snp 8.0E-06; 8.0E-06 0.700 1 1998 1998
dbSNP: rs16989673
rs16989673
1 20 50582819 3 prime UTR variant G/GG in-del 0.700 1 2002 2002
dbSNP: rs1799999
rs1799999
4 0.923 0.143 7 113878379 missense variant C/A snp 0.22 0.17 0.700 1 1995 1995
dbSNP: rs182552223
rs182552223
3 1.000 0.071 19 7141787 missense variant T/C snp 1.2E-04 0.700 1 1995 1995
dbSNP: rs35449651
rs35449651
3 1.000 0.071 7 113878300 missense variant G/T snp 1.4E-03 1.2E-03 0.700 1 1994 1994