#Chr	Start	End	Ref	Alt	CLINSIG	CLNDBN	CLNACC	CLNDSDB	CLNDSDBID
11	116692026	116692026	C	T	other	APOLIPOPROTEIN_A-IV_RARE_VARIANT\x2c_APOA4*3	RCV000019496.24	.	.
11	116701353	116701353	C	T	Pathogenic|other|Pathogenic	Hyperalphalipoproteinemia_2|Coronary_heart_disease|not_provided	RCV000019493.29|RCV000128448.1|RCV000419477.1	MedGen:OMIM|MedGen|MedGen	C3151467:614028|C0010068|CN221809
11	116701354	116701354	G	A	other|Pathogenic	Coronary_heart_disease|Hyperalphalipoproteinemia_2	RCV000128449.1|RCV000148017.3	MedGen|MedGen:OMIM	C0010068|C3151467:614028
11	116701560	116701560	G	A	other|Pathogenic	Coronary_heart_disease|Hyperalphalipoproteinemia_2	RCV000128450.1|RCV000148019.3	MedGen|MedGen:OMIM	C0010068|C3151467:614028
11	116701613	116701613	G	T	other|Pathogenic	Coronary_heart_disease|Hyperalphalipoproteinemia_2	RCV000128451.1|RCV000148018.3	MedGen|MedGen:OMIM	C0010068|C3151467:614028
11	116703532	116703532	A	G	Pathogenic	Hyperalphalipoproteinemia_2	RCV000019492.24	MedGen:OMIM	C3151467:614028
11	116703580	116703580	A	G	Pathogenic	Apolipoprotein_c-iii\x2c_nonglycosylated	RCV000019491.27	.	.