Remove clinvar duplicate variant

Author: bpblanken

v03_pipeline/var/test/reference_datasets/raw/clinvar.vcf

@@ -51,5 +51,4 @@
 1	925946	9	C	G	.	.	ALLELEID=1983057;CLNDISDB=MedGen:C3661900;CLNDN=not_provided;CLNHGVS=NC_000001.11:g.925946C>G;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Uncertain_significance;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=SAMD11:148398;MC=SO:0001583|missense_variant;ORIGIN=1
 1	925952	10	G	A	.	.	ALLELEID=1003021;CLNDISDB=MedGen:C3661900;CLNDN=not_provided;CLNHGVS=NC_000001.11:g.925952G>A;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Uncertain_significance;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=SAMD11:148398;MC=SO:0001583|missense_variant;ORIGIN=1;RS=1640863258
 1	925956	11	C	T	.	.	ALLELEID=1632777;CLNDISDB=MedGen:C3661900;CLNDN=not_provided;CLNHGVS=NC_000001.11:g.925956C>T;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Likely_benign;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=SAMD11:148398;MC=SO:0001819|synonymous_variant;ORIGIN=1;RS=1342334044
-1	925956	11	C	T	.	.	ALLELEID=1632777;CLNDISDB=MedGen:C3661900;CLNDN=not_provided;CLNHGVS=NC_000001.11:g.925956C>T;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Likely_benign;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=SAMD11:148398;MC=SO:0001819|synonymous_variant;ORIGIN=1;RS=1342334044
 MT	13112	693521	T	C	.	.	ALLELEID=680411;CLNDISDB=MONDO:MONDO:0009723,MedGen:C0023264,OMIM:256000,Orphanet:506;CLNDN=Leigh_syndrome;CLNHGVS=NC_012920.1:m.13112T>C;CLNREVSTAT=criteria_provided,_single_submitter;CLNSIG=Pathogenic;CLNVC=single_nucleotide_variant;CLNVCSO=SO:0001483;GENEINFO=MT-ND5:4540;ORIGIN=1;RS=1603224043