List of variants in gene THPO 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000460.4(THPO):c.469C>T (p.Arg157Ter)	rs1412486198	0.00001
NM_000460.4(THPO):c.13+1G>C	rs2108623965
NM_000460.4(THPO):c.13+1G>T
NM_000460.4(THPO):c.295C>T (p.Arg99Trp)

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