C1859648[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 626179	NM_013351.2(TBX21):c.83G>A (p.Gly28Asp)	LOC109286563, TBX21 (G28D)	Single nucleotide variant (missense variant)	Asthma, nasal polyps, and aspirin intolerance +1 more	GUncertain significance
Select item 2500097	NM_013351.2(TBX21):c.113C>A (p.Pro38Gln)	LOC109286563, TBX21 (P38Q)	Single nucleotide variant (missense variant)	Asthma, nasal polyps, and aspirin intolerance +1 more	GUncertain significance
Select item 828012	NM_013351.2(TBX21):c.326C>G (p.Ala109Gly)	LOC130061064, TBX21 (A109G)	Single nucleotide variant (missense variant)	Asthma, nasal polyps, and aspirin intolerance +1 more	GUncertain significance
Select item 992544	NM_013351.2(TBX21):c.1066T>C (p.Ser356Pro)	TBX21 (S356P)	Single nucleotide variant (missense variant)	Asthma, nasal polyps, and aspirin intolerance +1 more	GUncertain significance
Select item 992545	NM_013351.2(TBX21):c.1157G>T (p.Trp386Leu)	TBX21 (W386L)	Single nucleotide variant (missense variant)	Asthma, nasal polyps, and aspirin intolerance +1 more	GUncertain significance
Select item 626180	NM_013351.2(TBX21):c.1272G>T (p.Glu424Asp)	TBX21 (E424D)	Single nucleotide variant (missense variant)	Asthma, nasal polyps, and aspirin intolerance +1 more	GUncertain significance

ClinVar