List of variants in gene C8B reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000066.4(C8B):c.271C>T (p.Gln91Ter)	rs146187042	0.00023
NM_000066.4(C8B):c.1105+1G>A
NM_000066.4(C8B):c.1106-2A>G
NM_000066.4(C8B):c.1552+2T>C
NM_000066.4(C8B):c.1553-2A>G
NM_000066.4(C8B):c.249+2T>A
NM_000066.4(C8B):c.534-2A>G
NM_000066.4(C8B):c.865-1G>C
NM_000066.4(C8B):c.92+2T>A	rs2101487641

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