"GeneDx"[submitter] AND "PRDX1"[gene] - ClinVar

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57754	GRCh38/hg38 1p34.1(chr1:45402871-45603348)x3	AKR1A1, CCDC163 +22 more	Copy number gain	See cases	GUncertain significance
Select item 1251776	NM_181697.3(PRDX1):c.515-171_515-170del	MMACHC, PRDX1	Microsatellite (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1178886	NM_181697.3(PRDX1):c.261-195A>C	PRDX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225786	NM_181697.3(PRDX1):c.260+218C>T	PRDX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260318	NM_181697.3(PRDX1):c.260+182C>T	PRDX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278652	NM_181697.3(PRDX1):c.260+68T>C	PRDX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242857	NM_181697.3(PRDX1):c.107-33A>G	PRDX1	Single nucleotide variant (intron variant)	Cobalamin C disease +1 more	GBenign
Select item 1249354	NM_181697.3(PRDX1):c.107-36_107-35del	PRDX1	Microsatellite (intron variant)	not provided	GBenign
Select item 1252605	NM_181697.3(PRDX1):c.-11-129_-11-127del	PRDX1	Microsatellite (intron variant)	not provided	GBenign
Select item 253787	GRCh37/hg19 1p34.1(chr1:45953923-46126722)x3	AKR1A1, CCDC17 +5 more	Copy number gain	See cases	GUncertain significance