List of variants in gene CHRND reported as 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000751.3(CHRND):c.1006C>T (p.Arg336Ter)	rs754087173	0.00001
NM_000751.3(CHRND):c.127C>T (p.Arg43Trp)	rs55868108	0.00001
NM_000751.3(CHRND):c.234G>A (p.Trp78Ter)	rs121909505	0.00001
NM_000751.3(CHRND):c.521_524dup (p.Ala176fs)	rs1574630951	0.00001
NM_000751.3(CHRND):c.880C>T (p.Leu294Phe)	rs1574633904

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