Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs573658040 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs1275147925 1.000 0.080 19 44906613 missense variant A/G snv 7.0E-06 1
rs1458301734 1.000 0.080 19 44908687 missense variant G/A;T snv 5.9E-06 1
rs868094551 1.000 0.080 19 44908768 missense variant C/A;T snv 1