List of variants in gene REN reported as likely 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_000537.4(REN):c.145C>T (p.Arg49Ter)	rs121917741	0.00001
NM_000537.4(REN):c.249+1G>A	rs756544334	0.00001
NM_000537.4(REN):c.116T>A (p.Met39Lys)	rs1558245626
NM_000537.4(REN):c.249+1G>T

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