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: rs786201057
rs786201057
24 0.677 0.400 17 7675995 missense variant G/A;C;T snv 0.700 1.000 10 2003 2017
dbSNP: rs786201059
rs786201059
20 0.701 0.360 17 7673764 stop gained C/A;G;T snv 0.700 1.000 10 2000 2014
dbSNP: rs1057519747
rs1057519747
23 0.716 0.280 17 7675094 missense variant A/C;G;T snv 0.700 1.000 9 1995 2017
dbSNP: rs11540654
rs11540654
4 0.925 0.200 17 7676040 missense variant C/A;G;T snv 4.8E-05 0.700 1.000 9 1994 2014
dbSNP: rs28934576
rs28934576
78 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.700 1.000 9 2000 2017
dbSNP: rs397516435
rs397516435
6 0.851 0.280 17 7674945 stop gained G/A;C snv 4.0E-06 0.700 1.000 9 2001 2017
dbSNP: rs863224451
rs863224451
20 0.701 0.440 17 7673796 missense variant C/A;G;T snv 0.700 1.000 9 1993 2011
dbSNP: rs587781288
rs587781288
16 0.732 0.440 17 7675190 missense variant C/A;T snv 0.700 1.000 8 1999 2011
dbSNP: rs587781433
rs587781433
3 0.925 0.080 17 7674197 missense variant T/C;G snv 0.700 1.000 8 1995 2011
dbSNP: rs730882025
rs730882025
21 0.724 0.360 17 7674885 missense variant C/A;G;T snv 0.700 1.000 8 2000 2015
dbSNP: rs1057519989
rs1057519989
17 0.732 0.240 17 7674233 missense variant C/A;G;T snv 0.700 1.000 7 1996 2016
dbSNP: rs1057519992
rs1057519992
14 0.742 0.400 17 7674890 missense variant T/A;C;G snv 0.700 1.000 7 1995 2010
dbSNP: rs1131691023
rs1131691023
2 1.000 0.080 17 7675142 missense variant A/G;T snv 0.700 1.000 7 1994 2016
dbSNP: rs11540652
rs11540652
57 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 7 2001 2017
dbSNP: rs121913344
rs121913344
5 0.925 0.200 17 7673704 stop gained G/A;T snv 0.700 1.000 7 1997 2017
dbSNP: rs28934873
rs28934873
3 0.925 0.120 17 7675214 start lost A/G snv 0.700 1.000 7 1991 2011
dbSNP: rs730882029
rs730882029
4 0.882 0.200 17 7670685 stop gained G/A snv 0.700 1.000 7 2007 2016
dbSNP: rs751477326
rs751477326
3 1.000 0.080 17 7675082 missense variant G/A;C snv 4.0E-06 0.700 1.000 7 1995 2016
dbSNP: rs876659802
rs876659802
16 0.732 0.440 17 7673787 missense variant G/A;C;T snv 0.700 1.000 7 1996 2011
dbSNP: rs879253894
rs879253894
2 1.000 0.120 17 7674876 missense variant G/A snv 4.0E-06 0.700 1.000 7 1994 2015
dbSNP: rs879253942
rs879253942
28 0.677 0.400 17 7673826 missense variant A/G snv 0.700 1.000 7 1996 2011
dbSNP: rs985033810
rs985033810
16 0.724 0.280 17 7674232 missense variant C/A;G;T snv 0.700 1.000 7 1994 2015
dbSNP: rs1057519999
rs1057519999
12 0.763 0.160 17 7674247 missense variant T/C;G snv 0.700 1.000 6 1999 2010
dbSNP: rs1064793881
rs1064793881
3 0.925 0.120 17 7673784 missense variant C/T snv 0.700 1.000 6 1996 2009
dbSNP: rs1064795203
rs1064795203
2 1.000 0.120 17 7675080 missense variant G/C;T snv 0.700 1.000 6 2011 2017