List of variants in gene GFER reported as likely benign by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005262.3(GFER):c.*88C>T	rs61729107	0.00378
NM_005262.3(GFER):c.*3G>T	rs779641464	0.00006
NM_005262.3(GFER):c.270G>C (p.Lys90Asn)	rs863224024	0.00001
NM_005262.3(GFER):c.514C>A (p.His172Asn)	rs758350837	0.00001
NM_005262.3(GFER):c.456-9C>T	rs1016101367
NM_005262.3(GFER):c.617AG[3] (p.Ter206=)	rs776890492

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