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: rs267607147
rs267607147
2 0.925 0.120 12 109784379 missense variant G/A;C snv 0.700 0
dbSNP: rs267607148
rs267607148
4 0.882 0.120 12 109800639 missense variant C/T snv 0.700 0
dbSNP: rs267607149
rs267607149
5 0.851 0.120 12 109784385 missense variant C/T snv 0.700 0
dbSNP: rs267607150
rs267607150
2 0.925 0.080 12 109792671 missense variant T/C snv 0.700 0
dbSNP: rs369091875
rs369091875
2 0.925 0.240 11 6633485 missense variant C/G;T snv 1.1E-03 0.700 0
dbSNP: rs387906324
rs387906324
2 0.925 0.080 12 109808308 missense variant C/T snv 0.700 0
dbSNP: rs387906902
rs387906902
3 0.925 0.080 12 109793560 missense variant G/C;T snv 4.0E-06 0.700 0
dbSNP: rs387906903
rs387906903
2 0.925 0.120 12 109803113 missense variant T/C snv 0.700 0
dbSNP: rs387906904
rs387906904
5 0.851 0.080 12 109803009 missense variant G/A snv 0.700 0
dbSNP: rs387906906
rs387906906
3 0.925 0.120 12 109786827 missense variant G/A snv 0.700 0
dbSNP: rs387906907
rs387906907
3 0.925 0.120 12 109800645 missense variant T/C snv 0.700 0
dbSNP: rs397514473
rs397514473
2 0.925 0.120 12 109814531 missense variant G/A snv 0.700 0
dbSNP: rs397514474
rs397514474
3 0.925 0.120 12 109814565 missense variant C/A snv 0.700 0
dbSNP: rs515726152
rs515726152
2 0.925 0.120 12 109798742 missense variant C/A snv 0.700 0
dbSNP: rs515726153
rs515726153
1 1.000 0.040 12 109796638 missense variant T/C snv 0.700 0
dbSNP: rs515726154
rs515726154
1 1.000 0.040 12 109794406 inframe deletion AAG/- delins 0.700 0
dbSNP: rs515726155
rs515726155
1 1.000 0.040 12 109793945 inframe insertion -/GGA delins 0.700 0
dbSNP: rs515726157
rs515726157
2 1.000 0.040 12 109792704 missense variant T/C snv 0.700 0
dbSNP: rs515726158
rs515726158
2 0.925 0.120 12 109792702 missense variant A/G snv 0.700 0
dbSNP: rs515726159
rs515726159
2 0.925 0.080 12 109792689 missense variant A/G snv 0.700 0
dbSNP: rs515726160
rs515726160
2 0.925 0.080 12 109792678 missense variant C/A snv 0.700 0
dbSNP: rs515726161
rs515726161
2 0.925 0.120 12 109792664 missense variant G/C snv 0.700 0
dbSNP: rs515726162
rs515726162
2 0.925 0.120 12 109792403 missense variant G/T snv 0.700 0
dbSNP: rs515726163
rs515726163
2 0.925 0.120 12 109792401 missense variant A/G snv 0.700 0
dbSNP: rs515726164
rs515726164
2 0.925 0.080 12 109792379 missense variant C/T snv 0.700 0