List of variants in gene FOXRED1 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_017547.4(FOXRED1):c.124A>C (p.Lys42Gln)	rs148346044	0.00301
NM_017547.4(FOXRED1):c.435C>T (p.Val145=)	rs147235743	0.00111
NM_017547.4(FOXRED1):c.867C>T (p.Asn289=)	rs200551914	0.00003
NM_017547.4(FOXRED1):c.1020G>C (p.Pro340=)	rs143739550
NM_017547.4(FOXRED1):c.135G>T (p.Leu45=)
NM_017547.4(FOXRED1):c.471G>A (p.Ser157=)
NM_017547.4(FOXRED1):c.879C>A (p.Ala293=)

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