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: rs137853905
rs137853905
1 1.000 0.080 11 61958158 missense variant G/A snv 0.700 1.000 18 1998 2011
dbSNP: rs1445469923
rs1445469923
1 1.000 0.080 11 61955809 missense variant C/G snv 6.7E-06 0.700 1.000 18 1998 2011
dbSNP: rs199529046
rs199529046
2 0.925 0.080 11 61956964 missense variant T/C;G snv 6.8E-05 0.700 1.000 18 1998 2011
dbSNP: rs281865204
rs281865204
1 1.000 0.080 11 61951823 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865206
rs281865206
1 1.000 0.080 11 61951834 missense variant G/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865207
rs281865207
2 1.000 0.080 11 61951835 missense variant C/T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865208
rs281865208
1 1.000 0.080 11 61951838 missense variant A/G;T snv 4.0E-06 0.700 1.000 18 1998 2011
dbSNP: rs281865209
rs281865209
1 1.000 0.080 11 61951844 missense variant G/A;C snv 1.2E-05 0.700 1.000 18 1998 2011
dbSNP: rs281865210
rs281865210
1 1.000 0.080 11 61951853 missense variant C/T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865211
rs281865211
1 1.000 0.080 11 61951856 missense variant T/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865212
rs281865212
1 1.000 0.080 11 61951867 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865213
rs281865213
1 1.000 0.080 11 61951878 stop gained G/A;T snv 4.0E-06 0.700 1.000 18 1998 2011
dbSNP: rs281865215
rs281865215
1 1.000 0.080 11 61951880 missense variant G/A snv 1.4E-05 0.700 1.000 18 1998 2011
dbSNP: rs281865216
rs281865216
1 1.000 0.080 11 61951887 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865217
rs281865217
1 1.000 0.080 11 61951891 missense variant T/C snv 4.0E-06 0.700 1.000 18 1998 2011
dbSNP: rs281865221
rs281865221
1 1.000 0.080 11 61955194 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865224
rs281865224
1 1.000 0.080 11 61955744 missense variant C/A;T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865225
rs281865225
2 0.925 0.080 11 61955745 missense variant G/A;T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865226
rs281865226
1 1.000 0.080 11 61955758 missense variant G/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865227
rs281865227
1 1.000 0.080 11 61955767 missense variant C/A;T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865228
rs281865228
1 1.000 0.080 11 61955769 missense variant T/C;G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865229
rs281865229
1 1.000 0.080 11 61955771 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865230
rs281865230
1 1.000 0.080 11 61955774 missense variant T/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865231
rs281865231
1 1.000 0.080 11 61955780 missense variant G/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865232
rs281865232
1 1.000 0.080 11 61955782 missense variant C/A snv 0.700 1.000 18 1998 2011