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: rs3197999
rs3197999
13 0.724 0.250 3 49684099 missense variant G/A snp 0.26 0.26 0.800 4 2011 2017
dbSNP: rs3184504
rs3184504
55 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 0.800 3 2013 2017
dbSNP: rs3748816
rs3748816
5 0.846 0.179 1 2595307 missense variant A/G snp 0.41 0.45 0.800 3 2012 2017
dbSNP: rs7426056
rs7426056
5 0.821 0.107 2 203747335 intergenic variant A/G snp 0.81 0.800 3 2013 2017
dbSNP: rs11168249
rs11168249
7 0.821 0.107 12 47814585 intron variant T/C snp 0.49 0.800 2 2013 2017
dbSNP: rs11676348
rs11676348
7 0.784 0.143 2 218145423 intergenic variant C/G,T snp 0.50 0.800 2 2013 2017
dbSNP: rs12369214
rs12369214
5 0.821 0.107 12 106804833 intron variant G/A snp 0.40 0.800 2 2013 2017
dbSNP: rs13140464
rs13140464
1 1.000 0.036 4 122578590 regulatory region variant G/T snp 0.10 0.800 2 2013 2017
dbSNP: rs1788097
rs1788097
1 1.000 0.036 18 69876452 intron variant C/T snp 0.54 0.800 2 2013 2017
dbSNP: rs2836883
rs2836883
3 0.923 0.071 21 39094818 regulatory region variant G/A snp 0.23 0.800 2 2013 2017
dbSNP: rs4147359
rs4147359
1 1.000 0.036 10 6066476 intergenic variant G/A snp 0.34 0.800 2 2013 2017
dbSNP: rs56258221
rs56258221
1 1.000 0.036 6 90320722 T/C snp 0.12 0.800 2 2013 2017
dbSNP: rs60652743
rs60652743
1 1.000 0.036 19 46702450 intron variant A/G snp 0.16 0.800 2 2013 2017
dbSNP: rs7556897
rs7556897
6 0.821 0.107 2 227795396 intergenic variant C/G,T snp 0.69 0.800 2 2013 2017
dbSNP: rs7937682
rs7937682
1 1.000 0.036 11 111709215 intron variant G/A,C snp 3.2E-05; 0.25 0.800 2 2013 2017
dbSNP: rs1452787
rs1452787
2 0.923 0.036 18 55539976 intron variant A/G snp 0.25 0.800 1 2014 2014
dbSNP: rs4676410
rs4676410
15 0.715 0.214 2 240624322 intron variant G/A snp 0.26 0.800 1 2014 2014
dbSNP: rs6720394
rs6720394
1 1.000 0.036 2 111231795 intron variant T/G snp 0.12 0.800 1 2011 2011
dbSNP: rs1893592
rs1893592
7 0.784 0.179 21 42434957 missense variant A/C,G snp 0.27; 8.0E-06 0.24 0.700 2 2017 2017
dbSNP: rs1001007
rs1001007
5 0.821 0.107 3 46387167 intron variant A/G,T snp 0.62 0.700 1 2017 2017
dbSNP: rs1004234
rs1004234
5 0.821 0.107 5 132421409 intron variant A/G,T snp 0.86 0.700 1 2017 2017
dbSNP: rs10094579
rs10094579
5 0.821 0.107 8 89837077 regulatory region variant C/A snp 0.18 0.700 1 2017 2017
dbSNP: rs10510607
rs10510607
5 0.821 0.107 3 28244770 intron variant C/T snp 0.15 0.700 1 2017 2017
dbSNP: rs10743181
rs10743181
5 0.821 0.107 11 2208529 intergenic variant A/G snp 0.78 0.700 1 2017 2017
dbSNP: rs10748781
rs10748781
7 0.801 0.143 10 99523573 intergenic variant C/A,G snp 0.68; 3.2E-05 0.700 1 2017 2017