List of variants in gene EGFR reported as benign for Inflammatory skin and bowel disease, neonatal, 2

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_005228.5(EGFR):c.2709T>C (p.Thr903=)	rs1140475	0.89501
NM_005228.5(EGFR):c.1498+22A>T	rs1558544	0.68282
NM_005228.5(EGFR):c.2361G>A (p.Gln787=)	rs1050171	0.51617
NM_005228.5(EGFR):c.474C>T (p.Asn158=)	rs2072454	0.50662
NM_005228.5(EGFR):c.1887T>A (p.Thr629=)	rs2227984	0.33239
NM_005228.5(EGFR):c.1562G>A (p.Arg521Lys)	rs2227983	0.22212

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