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: rs9973676
rs9973676
2 1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs964184
rs964184
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2012 2012
dbSNP: rs9641609
rs9641609
2 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs9632885
rs9632885
2 1.000 0.040 9 22072639 intron variant G/A snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs9632884
rs9632884
6 0.851 0.160 9 22072302 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs944801
rs944801
4 0.882 0.120 9 22051671 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs944799
rs944799
2 1.000 0.040 9 22050614 intron variant A/G snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs944797
rs944797
5 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 0.700 1.000 2 2011 2013
dbSNP: rs9384331
rs9384331
2 1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs9349379
rs9349379
19 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.800 1.000 2 2011 2013
dbSNP: rs91
rs91
2 1.000 0.080 7 24409992 intron variant T/C snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs8181050
rs8181050
2 1.000 0.040 9 22064392 intron variant G/A;C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs8134546
rs8134546
2 1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs8089491
rs8089491
1 18 31763291 upstream gene variant G/A snv 5.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs7866783
rs7866783
2 1.000 0.040 9 22056360 non coding transcript exon variant A/G snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs7865618
rs7865618
11 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.700 1.000 2 2011 2013
dbSNP: rs7859727
rs7859727
3 1.000 0.080 9 22102166 intron variant C/T snv 0.57 0.700 1.000 2 2011 2013
dbSNP: rs7859362
rs7859362
2 9 22105928 intron variant T/C snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs7857345
rs7857345
4 0.925 0.080 9 22087474 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs7857118
rs7857118
1 9 22124141 intron variant A/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs7804216
rs7804216
2 1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs77934287
rs77934287
2 1.000 0.080 12 23071319 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs77757620
rs77757620
2 1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs7689240
rs7689240
2 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs76294234
rs76294234
2 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 0.700 1.000 1 2017 2017