Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766124888
BCR
1.000 0.080 22 23253817 missense variant C/A;G snv 4.0E-06; 4.0E-06 1
rs768288452
BCR ; RSPH14
1.000 0.080 22 23181822 missense variant A/G snv 4.1E-06 1
rs369488601
RSPH14 ; BCR
1.000 0.080 22 23181175 missense variant G/A;C snv 1.9E-05; 9.7E-05 1
rs775014154
RSPH14 ; BCR
1.000 0.080 22 23181637 missense variant C/T snv 5.8E-05 7.0E-05 1