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: rs121434390
rs121434390
2 0.925 0.080 11 101504634 missense variant G/T snv 0.800 1.000 11 2005 2016
dbSNP: rs121434391
rs121434391
1 1.000 0.080 11 101504541 missense variant T/C snv 4.8E-05 1.7E-04 0.800 1.000 11 2005 2016
dbSNP: rs121434392
rs121434392
1 1.000 0.080 11 101504161 missense variant A/T snv 0.800 1.000 11 2005 2016
dbSNP: rs121434394
rs121434394
1 1.000 0.080 11 101453068 missense variant G/A snv 0.800 1.000 11 2005 2016
dbSNP: rs121434395
rs121434395
2 0.925 0.080 11 101453062 missense variant C/T snv 0.800 1.000 11 2005 2016
dbSNP: rs146776939
rs146776939
3 0.882 0.080 11 101504595 missense variant T/C snv 2.0E-04 2.2E-04 0.700 1.000 11 2005 2016
dbSNP: rs777715086
rs777715086
1 1.000 0.080 11 101491605 missense variant C/T snv 3.2E-05 2.1E-05 0.700 1.000 11 2005 2016
dbSNP: rs779430565
rs779430565
3 0.882 0.080 11 101504316 missense variant T/A snv 1.2E-05 1.4E-05 0.700 1.000 11 2005 2016
dbSNP: rs121434393
rs121434393
1 1.000 0.080 11 101453674 stop gained T/A snv 0.700 0
dbSNP: rs1451194842
rs1451194842
1 1.000 0.080 11 101504445 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs1555003819
rs1555003819
1 1.000 0.080 11 101504451 missense variant T/C snv 0.700 0
dbSNP: rs771594597
rs771594597
1 1.000 0.080 11 101471253 missense variant A/G snv 2.0E-05 0.700 0