List of variants in gene TXNRD2 reported as benign for adrenocortical insufficiency

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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_006440.5(TXNRD2):c.1109T>C (p.Ile370Thr)	rs1139793	0.77627
NM_006440.5(TXNRD2):c.177C>T (p.Ala59=)	rs5748470	0.50192
NM_006440.5(TXNRD2):c.196G>T (p.Ala66Ser)	rs5748469	0.35646
NM_006440.5(TXNRD2):c.1086+17G>A	rs2239893	0.25106
NM_006440.5(TXNRD2):c.662+14G>A	rs9606176	0.13466
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=)	rs144584524	0.00266
NM_006440.5(TXNRD2):c.110A>T (p.Gln37Leu)	rs148092370	0.00150
NM_006440.5(TXNRD2):c.763G>C (p.Gly255Arg)	rs76079250
NM_006440.5(TXNRD2):c.949+437del	rs35599379

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