List of variants in gene RETREG1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_001034850.3(RETREG1):c.379C>T (p.Arg127Cys)	rs78314670	0.00642
NM_001034850.3(RETREG1):c.607G>A (p.Val203Met)	rs143878016	0.00296
NM_001034850.3(RETREG1):c.264C>T (p.Ser88=)	rs750040156	0.00004
NM_001034850.3(RETREG1):c.1089T>C (p.Asp363=)	rs200156015
NM_001034850.3(RETREG1):c.1404T>C (p.Ser468=)	rs1188421518

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