List of variants in gene combination APC, LOC129994371 reported by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NC_000005.10:g.112707478G>C	rs59923692	0.01117
NM_001127511.3(APC):c.-181C>T	rs115658307	0.00491
NM_001127511.3(APC):c.-188C>T	rs761454123	0.00004
NM_001127511.3(APC):c.-182G>A	rs1554060189
NM_001127511.3(APC):c.-191T>C	rs879253783
NM_001127511.3(APC):c.-207C>T

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