List of variants in gene FECH 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000140.5(FECH):c.913G>T (p.Val305Phe)	rs765518889	0.00002
NM_000140.5(FECH):c.286C>T (p.Arg96Ter)	rs984041251
NM_000140.5(FECH):c.463+1G>T	rs1206108637
NM_000140.5(FECH):c.463G>C (p.Ala155Pro)	rs2122320829
NM_000140.5(FECH):c.598+1dup
NM_000140.5(FECH):c.598+2T>G
NM_000140.5(FECH):c.705+1G>A
NM_000140.5(FECH):c.707G>A (p.Cys236Tyr)
NM_000140.5(FECH):c.791C>T (p.Ser264Leu)
NM_000140.5(FECH):c.805-1G>A	rs2122251187
NM_000140.5(FECH):c.913-2A>G

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