C5561926[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 39126	NM_198253.3(TERT):c.915G>A (p.Ala305=)	TERT	Single nucleotide variant (synonymous variant +1 more)	not provided +10 more	GBenign
Select item 227071	NM_001098668.4(SFTPA2):c.667C>A (p.Gln223Lys)	SFTPA2 (Q223K +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 227069	NM_001098668.4(SFTPA2):c.420C>T (p.Ser140=)	SFTPA2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1332949	NM_001098668.4(SFTPA2):c.292+21G>A	SFTPA2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1247340	NM_001098668.4(SFTPA2):c.-23-5G>A	SFTPA2	Single nucleotide variant (intron variant +1 more)	not provided +1 more	GBenign
Select item 1065526	NM_002458.3(MUC5B):c.2041A>G (p.Ser681Gly)	MUC5B (S681G)	Single nucleotide variant (missense variant)	Interstitial lung disease 2	GLikely benign
Select item 1065525	NM_002458.3(MUC5B):c.2045A>G (p.Asp682Gly)	MUC5B (D682G)	Single nucleotide variant (missense variant)	Interstitial lung disease 2	GLikely benign
Select item 403172	NM_002458.3(MUC5B):c.12537G>C (p.Gln4179His)	MUC5B, MUC5B-AS1 (Q4179H)	Single nucleotide variant (missense variant)	Interstitial lung disease 2 +2 more	GBenign

ClinVar