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: rs2301220
rs2301220
1 1.000 0.080 6 33070989 intron variant C/A;T snv 0.700 1.000 3 2009 2013
dbSNP: rs10484569
rs10484569
1 1.000 0.080 6 33091175 downstream gene variant G/A snv 5.9E-02 0.700 1.000 2 2009 2011
dbSNP: rs1431399
rs1431399
1 1.000 0.080 6 33073257 intron variant A/G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1431403
rs1431403
2 0.925 0.200 6 33079254 intron variant T/C snv 0.37 0.700 1.000 2 2012 2013
dbSNP: rs2281388
rs2281388
4 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 0.700 1.000 2 2009 2011
dbSNP: rs2647050
rs2647050
4 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 0.700 1.000 2 2011 2013
dbSNP: rs3117222
rs3117222
3 0.882 0.280 6 33093172 intron variant C/T snv 0.33 0.700 1.000 2 2009 2011
dbSNP: rs553665868
rs553665868
1 1.000 0.080 6 33080917 missense variant A/G snv 0.700 1.000 2 2013 2013
dbSNP: rs7773694
rs7773694
3 0.882 0.280 6 32738557 upstream gene variant A/G snv 0.80 0.700 1.000 2 2011 2013
dbSNP: rs9277554
rs9277554
7 0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 0.700 1.000 2 2011 2013
dbSNP: rs9469341
rs9469341
1 1.000 0.080 6 33068100 3 prime UTR variant A/C;G snv 0.700 1.000 2 2011 2013
dbSNP: rs10214910
rs10214910
1 1.000 0.080 6 33069898 intron variant C/A snv 0.23 0.32 0.700 1.000 1 2013 2013
dbSNP: rs10243492
rs10243492
1 1.000 0.080 7 32780825 intergenic variant A/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs10272859
rs10272859
4 0.925 0.120 7 90689160 intron variant G/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs1042190
rs1042190
1 1.000 0.080 6 33069222 missense variant T/C snv 0.24 0.28 0.700 1.000 1 2013 2013
dbSNP: rs1042544
rs1042544
2 0.925 0.200 6 33086680 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs11089620
rs11089620
1 1.000 0.080 22 21568167 non coding transcript exon variant C/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1110446
rs1110446
2 0.925 0.120 6 30103160 3 prime UTR variant C/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs1126542
rs1126542
1 1.000 0.080 6 33069647 missense variant T/A;C;G snv 0.24 0.28 0.700 1.000 1 2013 2013
dbSNP: rs1126769
rs1126769
1 1.000 0.080 6 33068658 missense variant T/G snv 0.24 0.29 0.700 1.000 1 2013 2013
dbSNP: rs11638027
rs11638027
1 1.000 0.080 15 90302268 intron variant G/T snv 9.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs11752643
rs11752643
2 0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs12484550
rs12484550
1 1.000 0.080 22 21587626 intron variant C/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2011 2011
dbSNP: rs12649554
rs12649554
1 1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65 0.700 1.000 1 2011 2011