ClinVar for MedGen (Select 358271) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2502178	NM_006895.3(HNMT):c.137+2287G>A	HNMT	Single nucleotide variant (intron variant)	Inherited susceptibility to asthma +1 more	GUncertain significance
Select item 445774	NM_006895.3(HNMT):c.475del (p.His159fs)	HNMT (H159fs)	Deletion (frameshift variant)	Inherited susceptibility to asthma +3 more	GConflicting classifications of pathogenicity
Select item 225964	NM_000594.3(TNF):c.-488G>A	TNF	Single nucleotide variant	etanercept response - Efficacy	Gdrug response
Select item 14673	NM_002188.3(IL13):c.431A>G (p.Gln144Arg)	IL13 (Q144R +1 more)	Single nucleotide variant (missense variant)	IL13-related disorder	GBenign
Select item 14672	NM_001354991.2(IL13):c.-93+487C>T	IL13	Single nucleotide variant (5 prime UTR variant +1 more)	Inherited susceptibility to asthma	Grisk factor
Select item 14055	IL12B, 4237G-A	IL12B	Single nucleotide variant	Inherited susceptibility to asthma	GUncertain significance
Select item 12253	NM_003357.5(SCGB1A1):c.-38=	SCGB1A1	Single nucleotide variant (no sequence alteration)	Inherited susceptibility to asthma	GUncertain significance
Select item 8368	NC_000017.11:g.34274816GAGAAG[9]	CCL11	Microsatellite	Inherited susceptibility to asthma	Grisk factor
Select item 5160	NM_006895.3(HNMT):c.314C>T (p.Thr105Ile)	HNMT (T105I)	Single nucleotide variant (missense variant)	HNMT-related disorder	GBenign
Select item 4253	NC_000005.10:g.147878599G>A	SCGB3A2	Single nucleotide variant	Inherited susceptibility to asthma	Grisk factor