Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727503741
VCL
1.000 0.040 10 74114349 stop gained C/T snv 2
rs1564526327
LOC107984244 ; VCL
10 74083453 frameshift variant T/- delins 1
rs781036800
VCL
10 74111991 frameshift variant CT/- del 1.3E-04 1
rs779488376
VCL
10 74095825 frameshift variant A/- del 4.0E-05 7.0E-06 1
rs727504381
VCL
10 74097222 stop gained C/T snv 1
rs727503738
VCL
10 74095654 splice acceptor variant A/G snv 1
rs397517244
VCL
10 74072792 stop gained C/T snv 1.2E-05 1.4E-05 1
rs397517245
VCL
10 74074773 frameshift variant -/A delins 1
rs876657674
VCL
10 74074789 frameshift variant -/G delins 1
rs863225121
VCL
1.000 0.080 10 74094449 missense variant G/T snv 1