List of variants in gene TXNRD2 reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_006440.5(TXNRD2):c.375-19T>G	rs147120537	0.00527
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=)	rs144584524	0.00266
NM_006440.5(TXNRD2):c.374+17G>A	rs200108545	0.00080
NM_006440.5(TXNRD2):c.592-17C>A	rs375350567	0.00044
NM_006440.5(TXNRD2):c.662+11C>G	rs373734411	0.00038
NM_006440.5(TXNRD2):c.229+15A>G	rs370756162	0.00029
NM_006440.5(TXNRD2):c.1275+18C>T	rs374333900	0.00023
NM_006440.5(TXNRD2):c.1086+12G>A	rs143966577	0.00021
NM_006440.5(TXNRD2):c.173-19del	rs770032943	0.00020
NM_006440.5(TXNRD2):c.1155G>C (p.Gly385=)	rs370957634	0.00019
NM_006440.5(TXNRD2):c.1276-15G>A	rs374202570	0.00014
NM_006440.5(TXNRD2):c.949+11G>A	rs772807846	0.00007
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=)	rs544242322	0.00006
NM_006440.5(TXNRD2):c.1445+13G>T	rs938029725	0.00006
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=)	rs767236339	0.00006
NM_006440.5(TXNRD2):c.528+19C>T	rs746285839	0.00006
NM_006440.5(TXNRD2):c.1182+19C>T	rs377040175	0.00004
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=)	rs372816982	0.00003
NM_006440.5(TXNRD2):c.1497A>G (p.Thr499=)	rs969582646	0.00003
NM_006440.5(TXNRD2):c.449+17C>T	rs370505160	0.00003
NM_006440.5(TXNRD2):c.489C>T (p.Asp163=)	rs751116028	0.00003
NM_006440.5(TXNRD2):c.1086+11C>T	rs369332144	0.00002
NM_006440.5(TXNRD2):c.172+20C>A	rs760016716	0.00001
NM_006440.5(TXNRD2):c.588G>A (p.Thr196=)	rs377699868	0.00001
NM_006440.5(TXNRD2):c.1107C>A (p.Pro369=)	rs371533709
NM_006440.5(TXNRD2):c.173-15T>C	rs1555913241
NM_006440.5(TXNRD2):c.450-15_450-14del	rs767787404
NM_006440.5(TXNRD2):c.529-8C>T	rs754998172
NM_006440.5(TXNRD2):c.592-20G>C	rs1555911999
NM_006440.5(TXNRD2):c.592-5G>C	rs1555911995
NM_006440.5(TXNRD2):c.682+16G>A	rs377147143

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