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: rs104894313
rs104894313
7 0.807 0.160 11 89284805 missense variant C/T snv 3.8E-03; 4.0E-06 3.7E-03 0.700 0
dbSNP: rs104894314
rs104894314
8 0.790 0.160 11 89191205 missense variant G/A;T snv 8.0E-06; 9.2E-05 0.700 0
dbSNP: rs121908011
rs121908011
6 0.827 0.160 11 89227933 missense variant G/A snv 9.2E-05 3.5E-05 0.700 0
dbSNP: rs28940879
rs28940879
5 0.851 0.160 11 89178117 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs28940881
rs28940881
16 0.776 0.200 11 89177954 start lost A/G snv 6.4E-05 5.6E-05 0.700 0
dbSNP: rs61753180
rs61753180
4 0.882 0.160 11 89178093 missense variant G/A snv 1.6E-04 2.8E-04 0.700 0
dbSNP: rs61753256
rs61753256
4 0.882 0.160 11 89178299 stop gained C/A;T snv 4.0E-06; 2.4E-05 0.700 0
dbSNP: rs61754381
rs61754381
8 0.790 0.200 11 89227816 splice region variant T/A;C snv 9.5E-04; 8.0E-06 0.700 0
dbSNP: rs61754388
rs61754388
6 0.827 0.160 11 89227904 missense variant C/A snv 3.4E-04 5.0E-04 0.700 0
dbSNP: rs62645904
rs62645904
8 0.827 0.160 11 89191214 stop gained C/A;T snv 1.9E-04 0.700 0
dbSNP: rs62645916
rs62645916
4 0.882 0.160 11 89284787 stop gained G/A;T snv 3.6E-05 0.700 0
dbSNP: rs63159160
rs63159160
4 0.882 0.160 11 89178602 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.700 0
dbSNP: rs1126809
rs1126809
29 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 0.010 1.000 1 1997 1997
dbSNP: rs1376096651
rs1376096651
3 0.882 0.280 3 69964977 missense variant A/G;T snv 0.010 1.000 1 1997 1997