Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 10
rs150516929
CRYAB
0.807 0.240 11 111908832 missense variant C/T snv 9.1E-04 8.7E-04 7
rs387907338
HSPB2-C11orf52 ; HSPB2 ; CRYAB
0.827 0.200 11 111911559 missense variant G/A;T snv 4
rs141638421
CRYAB
0.882 0.080 11 111908822 missense variant C/T snv 7.2E-05 4.9E-05 3
rs370803064
CRYAB
0.925 0.200 11 111908781 missense variant C/T snv 4.0E-06 7.0E-06 3
rs387907339
CRYAB
0.882 0.280 11 111908967 missense variant C/A;G snv 3
rs534473091
CRYAB
0.882 0.040 11 111908925 missense variant G/A snv 2.0E-05 4.9E-05 3
rs781902168
HSPB2 ; CRYAB ; HSPB2-C11orf52
0.882 0.040 11 111911694 missense variant G/A;C snv 3.2E-05 3
rs139750142
CRYAB
0.925 0.200 11 111910446 missense variant G/A;T snv 9.5E-05; 4.0E-06 6.3E-05 2
rs375933774
CRYAB ; HSPB2-C11orf52 ; HSPB2
0.925 0.040 11 111911691 missense variant G/A snv 2.3E-05 3.5E-05 2
rs782809283
HSPB2 ; CRYAB ; HSPB2-C11orf52
1.000 0.040 11 111911693 missense variant C/T snv 1.8E-05 4.2E-05 1