Related gene-specific medical variations for Gene (Select 4259) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294644	NM_004528.4(MGST3):c.134G>A (p.Ser45Asn)	LOC126805899, MGST3 (S45N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411675	NM_004528.4(MGST3):c.176G>A (p.Arg59Gln)	LOC126805899, MGST3 (R59Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1693602	NM_004528.4(MGST3):c.192-423G>A	LOC126805899, MGST3	Single nucleotide variant (intron variant)	Pulmonary disease, chronic obstructive, susceptibility to	Gassociation

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