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: rs16917667
rs16917667
3 1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02 0.700 1.000 2 2018 2019
dbSNP: rs365990
rs365990
4 1.000 0.080 14 23392602 missense variant A/G snv 0.34 0.45 0.800 1.000 2 2010 2013
dbSNP: rs10002082
rs10002082
1 4 164159753 intron variant A/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10142635
rs10142635
1 14 34423401 intron variant A/G snv 3.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs1015003
rs1015003
1 8 37238541 intergenic variant G/T snv 0.58 0.800 1.000 1 2013 2013
dbSNP: rs1015451
rs1015451
1 6 121810339 intergenic variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs10517800
rs10517800
1 4 164174438 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11006544
rs11006544
3 1.000 0.040 10 59510886 intergenic variant T/C snv 7.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs11034161
rs11034161
1 11 37475966 intergenic variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs11065706
rs11065706
1 12 110717726 downstream gene variant T/C snv 0.19 0.800 1.000 1 2013 2013
dbSNP: rs11110004
rs11110004
3 1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs11118555
rs11118555
1 1 207767508 non coding transcript exon variant T/A snv 9.3E-02 0.800 1.000 1 2013 2013
dbSNP: rs11153730
rs11153730
4 6 118346359 intergenic variant T/C snv 0.40 0.800 1.000 1 2013 2013
dbSNP: rs11154027
rs11154027
3 1.000 0.080 6 121460244 intergenic variant T/C snv 0.61 0.800 1.000 1 2013 2013
dbSNP: rs1120384
rs1120384
1 4 164161744 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs112434206
rs112434206
3 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs113235453
rs113235453
3 1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs114821210
rs114821210
3 1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs11578508
rs11578508
1 1 207955720 upstream gene variant A/G snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs11645781
rs11645781
1 16 6846127 intron variant A/C;G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs11930019
rs11930019
1 4 164159224 intron variant T/C snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs11931264
rs11931264
1 4 164160251 intron variant T/C snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs11943491
rs11943491
1 4 164159378 intron variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11968176
rs11968176
1 6 118579777 intron variant C/A snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs12110693
rs12110693
2 6 121837124 intergenic variant G/A snv 0.23 0.700 1.000 1 2009 2009