List of variants in gene MTRR reported as likely benign for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_002454.3(MTRR):c.739C>T (p.Pro247Ser)	rs114053717	0.00190
NM_002454.3(MTRR):c.869T>C (p.Ile290Thr)	rs144899305	0.00092
NM_002454.3(MTRR):c.1182C>G (p.Asp394Glu)	rs149678769	0.00041
NM_002454.3(MTRR):c.904-4C>G	rs370809675	0.00018
NM_002454.3(MTRR):c.346C>A (p.Gln116Lys)	rs202110383	0.00014
NM_002454.3(MTRR):c.1537G>A (p.Gly513Arg)	rs150411351	0.00006
NM_002454.3(MTRR):c.1135A>G (p.Ile379Val)	rs746404785	0.00001
NM_002454.3(MTRR):c.1033A>G (p.Ile345Val)	rs2478946105
NM_002454.3(MTRR):c.1910C>T (p.Ala637Val)	rs764159535

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