List of variants in gene combination LOC107303340, VHL reported as benign by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.340+648T>C	rs73024533	0.01009
NM_000551.4(VHL):c.463+8C>T	rs5030834	0.00051
NM_000551.4(VHL):c.340+679T>G	rs866935879	0.00037
NM_000551.4(VHL):c.*70C>T	rs552290225	0.00011
NM_000551.4(VHL):c.340+837A>G	rs190906863	0.00006
NM_000551.4(VHL):c.340+621T>C	rs562162481	0.00005
NM_000551.4(VHL):c.340+724G>C	rs900590059	0.00002
NM_000551.4(VHL):c.340+595C>T	rs1335472800	0.00001
NM_000551.4(VHL):c.463+20dup
NM_000551.4(VHL):c.463+37_463+39del	rs869025658

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