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: rs10980800
rs10980800
3 9 111153625 intron variant T/C snv 0.21 0.700 1.000 3 2011 2017
dbSNP: rs2124440
rs2124440
2 2 181463487 intron variant G/A snv 0.55 0.700 1.000 3 2013 2017
dbSNP: rs10980797
rs10980797
3 9 111150273 intron variant A/G;T snv 0.700 1.000 2 2016 2018
dbSNP: rs1892548
rs1892548
2 13 40428504 intron variant T/A;C snv 0.700 1.000 2 2016 2018
dbSNP: rs1991866
rs1991866
3 8 129611859 intron variant G/A;C snv 0.700 1.000 2 2014 2017
dbSNP: rs445
rs445
9 7 92779056 intron variant C/T snv 0.14 0.700 1.000 2 2016 2018
dbSNP: rs4970966
rs4970966
2 1 150611627 intron variant G/T snv 0.16 0.700 1.000 2 2016 2018
dbSNP: rs76428106
rs76428106
10 0.851 0.040 13 28029870 intron variant T/C;G snv 0.700 1.000 2 2016 2017
dbSNP: rs10098310
rs10098310
3 8 129601368 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10147992
rs10147992
3 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10168795
rs10168795
2 2 224888625 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs1037171
rs1037171
2 17 74706839 intron variant G/A snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs10562650
rs10562650
2 2 181459460 intron variant TT/-;T;TTT delins 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10956483
rs10956483
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1105527
rs1105527
2 17 27521170 intron variant C/T snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs11189181
rs11189181
2 10 97384397 intron variant A/G snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs112505971
rs112505971
13 10 27068541 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11327184
rs11327184
4 8 129592027 intron variant C/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs113760175
rs113760175
3 6 22343363 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs114208039
rs114208039
2 6 31273862 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs115007843
rs115007843
2 4 82654059 intron variant A/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs115340020
rs115340020
2 1 92300881 intron variant G/A snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs11580646
rs11580646
2 1 117619797 intron variant C/G snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs11642657
rs11642657
3 16 85982722 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11723763
rs11723763
2 4 144137143 intron variant G/T snv 0.36 0.700 1.000 1 2016 2016