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: rs200688486
rs200688486
1 6 32621223 regulatory region variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs12154141
rs12154141
1 6 62460168 downstream gene variant A/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs9267536
rs9267536
1 6 31683417 intron variant A/C snv 5.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs28366298
rs28366298
3 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs8084
rs8084
2 1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 0.700 1.000 1 2013 2013
dbSNP: rs11229
rs11229
6 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 0.700 1.000 1 2013 2013
dbSNP: rs1800871
rs1800871
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.010 1.000 1 2012 2012
dbSNP: rs204995
rs204995
2 1.000 0.120 6 32186508 non coding transcript exon variant A/G snv 0.21 0.27 0.700 1.000 1 2013 2013
dbSNP: rs204999
rs204999
13 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs2213586
rs2213586
2 1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs3117583
rs3117583
3 0.925 0.200 6 31651799 5 prime UTR variant A/G snv 0.14 0.17 0.700 1.000 1 2013 2013
dbSNP: rs3130070
rs3130070
1 6 31624031 intron variant A/G snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs3130626
rs3130626
2 1.000 0.120 6 31630712 synonymous variant A/G snv 0.15 0.17 0.700 1.000 1 2013 2013
dbSNP: rs652888
rs652888
10 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 0.700 1.000 1 2013 2013
dbSNP: rs7195
rs7195
2 1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs2736157
rs2736157
2 1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17 0.700 1.000 1 2013 2013
dbSNP: rs2854275
rs2854275
4 0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs2239802
rs2239802
4 0.882 0.200 6 32444069 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2239803
rs2239803
4 0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs3130618
rs3130618
7 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs4919510
rs4919510
32 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 0.010 1.000 1 2015 2015
dbSNP: rs10885
rs10885
1 6 31636814 missense variant C/T snv 0.14 0.17 0.700 1.000 1 2013 2013
dbSNP: rs10947262
rs10947262
3 0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs204994
rs204994
4 0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2153486
rs2153486
1 14 87737048 intron variant C/T snv 0.68 0.700 1.000 1 2017 2017