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: rs12898370
rs12898370
3 1.000 0.080 15 77516256 intergenic variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1787395
rs1787395
3 1.000 0.080 21 37664176 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3764435
rs3764435
5 0.827 0.120 9 72901960 intron variant A/C;T snv 0.010 1.000 1 2011 2011
dbSNP: rs6701037
rs6701037
3 1.000 0.080 1 175150943 downstream gene variant A/C;T snv 0.800 1.000 1 2011 2011
dbSNP: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.100 0.893 28 1998 2019
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.030 1.000 3 2006 2018
dbSNP: rs1000579
rs1000579
3 1.000 0.080 4 4717767 intron variant A/G snv 0.44 0.800 1.000 2 2012 2017
dbSNP: rs2235751
rs2235751
3 0.882 0.120 20 1989288 intron variant A/G snv 0.40 0.020 1.000 2 2013 2017
dbSNP: rs3027172
rs3027172
2 0.925 0.080 17 8152405 missense variant A/G snv 0.38 0.17 0.020 1.000 2 2011 2015
dbSNP: rs886205
rs886205
8 0.827 0.360 12 111766623 intron variant A/G snv 0.35 0.020 1.000 2 2016 2017
dbSNP: rs9886351
rs9886351
2 0.925 0.080 7 70783483 non coding transcript exon variant A/G snv 0.33 0.020 1.000 2 2016 2017
dbSNP: rs10211296
rs10211296
3 1.000 0.080 2 165633833 intron variant A/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs1057302
rs1057302
1 1.000 0.080 1 175157287 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs10892169
rs10892169
1 1.000 0.080 11 117762339 intron variant A/G snv 0.68 0.010 1.000 1 2011 2011
dbSNP: rs111576572
rs111576572
3 1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs1116313
rs1116313
1 1.000 0.080 11 113425385 intron variant A/G snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs115357105
rs115357105
4 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs11825659
rs11825659
4 0.925 0.080 11 133925624 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11922615
rs11922615
1 1.000 0.080 3 9416623 intron variant A/G snv 8.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs12392447
rs12392447
1 1.000 0.080 X 154496001 non coding transcript exon variant A/G snv 0.700 1.000 1 2009 2009
dbSNP: rs12427267
rs12427267
1 1.000 0.080 12 91930196 intergenic variant A/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs12482570
rs12482570
3 1.000 0.080 21 37705475 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs12916379
rs12916379
1 1.000 0.080 15 38699319 non coding transcript exon variant A/G snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs139438618
rs139438618
5 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 0.710 1.000 1 2017 2017
dbSNP: rs1427074798
rs1427074798
1 1.000 0.080 10 100297067 synonymous variant A/G snv 4.0E-06 0.010 1.000 1 2008 2008