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: rs1179351306
rs1179351306
1 1.000 0.040 20 49374576 stop gained G/A;C snv 8.0E-06 0.700 0
dbSNP: rs1555889090
rs1555889090
1 1.000 0.040 20 49374416 missense variant C/G;T snv 0.700 0
dbSNP: rs1555889108
rs1555889108
2 0.925 0.040 20 49374559 missense variant A/G snv 0.700 0
dbSNP: rs1555889127
rs1555889127
6 1.000 0.040 20 49374625 missense variant C/T snv 0.700 0
dbSNP: rs1555889130
rs1555889130
3 0.882 0.040 20 49374644 missense variant G/A snv 0.700 0
dbSNP: rs1555889162
rs1555889162
6 0.882 0.040 20 49374931 missense variant G/A;C snv 0.700 0
dbSNP: rs1568658507
rs1568658507
1 1.000 0.040 20 49482353 missense variant T/C snv 0.700 0
dbSNP: rs1569017015
rs1569017015
1 1.000 0.040 20 49374312 missense variant G/T snv 0.700 0
dbSNP: rs1569017045
rs1569017045
1 1.000 0.040 20 49374359 missense variant C/T snv 0.700 0
dbSNP: rs1569017073
rs1569017073
1 1.000 0.040 20 49374380 missense variant C/T snv 0.700 0
dbSNP: rs1569017123
rs1569017123
1 1.000 0.040 20 49374421 missense variant T/C snv 0.700 0
dbSNP: rs1569017143
rs1569017143
1 1.000 0.040 20 49374428 missense variant C/G snv 0.700 0
dbSNP: rs1569017148
rs1569017148
1 1.000 0.040 20 49374430 missense variant G/T snv 0.700 0
dbSNP: rs1569017174
rs1569017174
1 1.000 0.040 20 49374455 missense variant A/G snv 0.700 0
dbSNP: rs1569017205
rs1569017205
1 1.000 0.040 20 49374515 missense variant C/A snv 0.700 0
dbSNP: rs1569017257
rs1569017257
1 1.000 0.040 20 49374592 missense variant G/A snv 0.700 0
dbSNP: rs1569017337
rs1569017337
1 1.000 0.040 20 49374703 frameshift variant A/- del 0.700 0
dbSNP: rs587777848
rs587777848
3 0.882 0.040 20 49374519 missense variant G/C;T snv 0.700 0
dbSNP: rs959316981
rs959316981
2 0.925 0.040 20 49374377 missense variant C/T snv 0.700 0