ClinVar Miner

List of variants reported as likely benign for Inflammatory skin and bowel disease, neonatal, 2; Lung cancer by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.3485G>A (p.Ser1162Asn)	rs41321844	0.00362
NM_005228.5(EGFR):c.968T>C (p.Val323Ala)	rs367680488	0.00018
NM_005228.5(EGFR):c.2709_2710inv (p.Val904Ile)

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