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: rs10491003
rs10491003
2 10 9286688 non coding transcript exon variant C/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs1067
rs1067
2 3 122414118 3 prime UTR variant G/A snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs10934582
rs10934582
3 3 122294507 downstream gene variant G/A snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs11101061
rs11101061
1 10 49244632 intergenic variant T/A snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs11105380
rs11105380
1 12 89702020 intron variant T/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs11918240
rs11918240
1 3 122226991 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11929034
rs11929034
2 3 122560202 intron variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs11967485
rs11967485
2 6 156807123 intron variant G/A snv 0.15 0.800 1.000 1 2013 2013
dbSNP: rs12107092
rs12107092
2 3 122405001 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs12150338
rs12150338
2 17 1730810 synonymous variant C/G;T snv 4.0E-06; 0.12 0.800 1.000 1 2010 2010
dbSNP: rs12517041
rs12517041
1 5 23301799 downstream gene variant A/G snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs12635478
rs12635478
2 3 122289706 3 prime UTR variant C/A snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs12780111
rs12780111
1 10 9254687 regulatory region variant G/C snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs12901379
rs12901379
1 15 50692447 downstream gene variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13068893
rs13068893
1 3 122307242 regulatory region variant C/G snv 8.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs13085498
rs13085498
2 3 122292516 downstream gene variant C/A;T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs13085674
rs13085674
2 3 122292504 downstream gene variant G/A snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs13095172
rs13095172
2 3 122271410 intron variant C/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs13103813
rs13103813
1 4 3466709 intron variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs13301969
rs13301969
1 9 126532675 downstream gene variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs1402200
rs1402200
2 3 122303570 intergenic variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs1472621
rs1472621
2 3 122293879 downstream gene variant A/G snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs1550532
rs1550532
4 2 233356202 intron variant C/G snv 0.75 0.800 1.000 1 2013 2013
dbSNP: rs16832956
rs16832956
2 3 122298661 regulatory region variant C/G;T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs16833078
rs16833078
2 3 122380747 intron variant A/G;T snv 0.700 1.000 1 2010 2010