Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 21
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 7
rs116928232 0.827 0.120 10 89222511 missense variant C/G;T snv 1.2E-05; 9.1E-04 7
rs111033560 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 7
rs267607277 0.807 0.120 14 90404386 missense variant A/G snv 3
rs730880082
DSP
0.882 0.120 6 7576986 stop gained C/G;T snv 3
rs12720459 0.807 0.160 11 2583535 missense variant C/A;G;T snv 3
rs587782933 0.827 0.200 12 2504526 missense variant G/A snv 2
rs79891110 0.807 0.320 12 2504944 stop gained G/A;T snv 2
rs755221106 0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 2
rs786205745 0.807 0.320 12 2504538 missense variant G/A;C snv 1
rs80315385 0.882 0.200 12 2504932 missense variant G/A snv 1
rs398124647 0.807 0.120 2 47161851 missense variant T/A;C snv 1
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 1
rs587777598 0.851 0.200 6 79921662 missense variant C/G;T snv 1
rs104894393 0.925 0.120 13 101726785 missense variant A/G snv 1
rs120074192 0.763 0.120 11 2527959 missense variant A/G snv 1
rs11567847 0.925 0.120 11 12937202 missense variant T/C snv 1
rs606231451 0.925 0.120 1 1535372 missense variant G/A snv 1