Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs398122820
B2M
0.790 0.240 15 44715641 missense variant G/A snv 2
rs863225287
B2M ; PATL2
1.000 0.080 15 44711614 splice donor variant G/T snv 1
rs104894481
PATL2 ; B2M
1.000 0.080 15 44711577 missense variant G/C;T snv 4.0E-06 1