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: rs80358284
rs80358284
10 0.790 0.240 11 86952443 missense variant T/A;C snv 4.0E-06; 2.4E-05 0.800 1.000 13 2002 2010
dbSNP: rs80358292
rs80358292
1 1.000 0.080 11 86951751 missense variant C/G snv 0.800 1.000 13 2002 2010
dbSNP: rs80358293
rs80358293
1 1.000 0.080 11 86951732 missense variant T/C snv 4.0E-06 0.800 1.000 13 2002 2010
dbSNP: rs80358294
rs80358294
3 0.882 0.080 11 86951506 missense variant C/G;T snv 1.2E-05 0.800 1.000 13 2002 2010
dbSNP: rs104894223
rs104894223
2 0.925 0.080 11 86951990 missense variant T/C snv 5.1E-04 5.2E-04 0.700 1.000 13 2002 2010
dbSNP: rs80358285
rs80358285
1 1.000 0.080 11 86952442 missense variant A/G snv 0.700 1.000 13 2002 2010
dbSNP: rs80358286
rs80358286
1 1.000 0.080 11 86952287 missense variant T/C snv 0.700 1.000 13 2002 2010
dbSNP: rs80358287
rs80358287
2 0.925 0.080 11 86952215 missense variant A/G snv 0.700 1.000 13 2002 2010
dbSNP: rs80358288
rs80358288
1 1.000 0.080 11 86952146 missense variant A/G snv 0.700 1.000 13 2002 2010
dbSNP: rs80358297
rs80358297
1 1.000 0.080 11 86951423 missense variant T/G snv 0.700 1.000 13 2002 2010
dbSNP: rs80358298
rs80358298
1 1.000 0.080 11 86951293 missense variant C/T snv 0.700 1.000 13 2002 2010
dbSNP: rs80358300
rs80358300
1 1.000 0.080 11 86951266 missense variant G/A;C snv 1.6E-05 0.700 1.000 13 2002 2010
dbSNP: rs1064794064
rs1064794064
1 1.000 0.080 11 86952145 missense variant C/T snv 0.700 0
dbSNP: rs80358301
rs80358301
1 1.000 0.080 11 86951272 inframe deletion CCACAT/- delins 0.700 0
dbSNP: rs80358303
rs80358303
1 1.000 0.080 11 86951254 frameshift variant AG/- delins 0.700 0