List of variants in gene C6 reported as likely pathogenic for not provided

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000065.5(C6):c.2381+2T>C	rs76202909	0.00242
NM_000065.5(C6):c.1138del (p.Gln380fs)	rs375762365	0.00206
NM_000065.5(C6):c.2291-1G>A	rs759338755	0.00008
NM_000065.5(C6):c.1333C>T (p.Arg445Ter)	rs778044260	0.00003
NM_000065.5(C6):c.2290+1G>T	rs769828883	0.00001
NC_000005.9:g.(?_41155054)_(41176837_?)dup
NC_000005.9:g.(?_41195874)_(41196055_?)dup
NM_000065.5(C6):c.1168+1G>T	rs2150311349
NM_000065.5(C6):c.1439_1458+10delinsAATTTTG
NM_000065.5(C6):c.1458+2T>A
NM_000065.5(C6):c.1968+1G>T	rs2150258844
NM_000065.5(C6):c.2049C>G (p.Tyr683Ter)	rs867425110
NM_000065.5(C6):c.2335_2336del (p.Gln779fs)	rs771792933
NM_000065.5(C6):c.446-1G>A
NM_000065.5(C6):c.727-2A>G
NM_000065.5(C6):c.927+1G>T	rs546788276

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