Related gene-specific medical variations for Gene (Select 7001) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3218488	NM_005809.6(PRDX2):c.253G>T (p.Ala85Ser)	LOC130063668, PRDX2 (A85S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218487	NM_005809.6(PRDX2):c.249C>A (p.His83Gln)	LOC130063668, PRDX2 (H83Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218486	NM_005809.6(PRDX2):c.182G>A (p.Arg61His)	LOC130063668, PRDX2 (R61H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3218485	NM_005809.6(PRDX2):c.136G>A (p.Asp46Asn)	LOC130063668, PRDX2 (D46N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253823	NM_005809.6(PRDX2):c.143C>G (p.Thr48Ser)	LOC130063668, PRDX2 (T48S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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