Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918284
BEST1 ; LOC107984334
0.882 0.080 11 61955892 missense variant G/A snv 5.2E-04 3.3E-04 5
rs281865238
BEST1 ; LOC107984334
0.851 0.080 11 61957402 missense variant C/A;T snv 4
rs753614067
BEST1 ; LOC107984334
1.000 0.080 11 61955870 missense variant C/G snv 3.3E-05 1.4E-05 3
rs374772670
FTH1 ; BEST1
0.882 0.160 11 61962313 missense variant G/A snv 8.0E-06 2.8E-05 3
rs121918288
BEST1
0.925 0.080 11 61951928 missense variant T/C snv 2.0E-05 7.0E-06 2
rs199529046
BEST1 ; LOC107984334
0.925 0.080 11 61956964 missense variant T/C;G snv 6.8E-05 2
rs281865258
BEST1 ; LOC107984334
0.925 0.080 11 61959528 missense variant G/A snv 2
rs765998048
BEST1 ; LOC107984334
0.925 0.080 11 61956966 missense variant C/T snv 1.6E-05 2
rs762398929
FTH1 ; BEST1
0.925 0.080 11 61962704 stop gained C/G snv 2.0E-05 2
rs200277476
LOC107984334 ; BEST1
0.925 0.080 11 61956946 missense variant C/T snv 2.6E-04 1.5E-04 2
rs267606678
LOC107984334 ; BEST1
0.925 0.080 11 61955888 missense variant C/G snv 3.3E-05 2
rs267606680
LOC107984334 ; BEST1
0.925 0.080 11 61956976 missense variant T/C snv 2
rs281865223
LOC107984334 ; BEST1
0.925 0.080 11 61955742 missense variant C/A;T snv 6.9E-06 2
rs281865225
LOC107984334 ; BEST1
0.925 0.080 11 61955745 missense variant G/A;T snv 2
rs281865277
LOC107984334 ; BEST1
0.925 0.080 11 61959564 missense variant G/A snv 4.8E-05 7.0E-06 2
rs28940273
LOC107984334 ; BEST1
0.925 0.080 11 61955749 stop gained G/A;C snv 2
rs771898125
BEST1
1.000 0.080 11 61951908 synonymous variant C/T snv 1.2E-05 2.1E-05 1
rs1554964287
BEST1 ; FTH1
1.000 0.080 11 61962524 missense variant C/G snv 1
rs121918286
BEST1 ; LOC107984334
1.000 0.080 11 61956960 stop gained C/T snv 1.2E-05 3.5E-05 1
rs1431752515
BEST1 ; LOC107984334
1.000 0.080 11 61957434 missense variant C/G snv 4.0E-06 1
rs775283269
BEST1 ; LOC107984334
1.000 0.080 11 61957408 stop gained C/A;T snv 8.0E-06; 8.0E-06 1
rs121918287
BEST1 ; LOC107984334 ; FTH1
1.000 0.080 11 61959892 missense variant G/A snv 1
rs368387447
BEST1 ; LOC107984334 ; FTH1
1.000 0.080 11 61959917 missense variant T/C snv 4.8E-05 6.3E-05 1
rs752521456
FTH1 ; BEST1
1.000 0.080 11 61962666 frameshift variant TG/- delins 2.0E-05 1
rs1417478879
LOC107984334 ; BEST1
1.000 0.080 11 61955924 missense variant C/G snv 2.7E-05 7.0E-06 1