List of variants in gene STRC reported as pathogenic for chromosomal disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_153700.2(STRC):c.3670C>T (p.Arg1224Ter)	rs727503444	0.00007
NM_153700.2(STRC):c.4351C>T (p.Arg1451Ter)	rs778909195	0.00001
NM_153700.2(STRC):c.461del (p.Pro154fs)	rs1411667337

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