List of variants in gene TXNRD2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006440.5(TXNRD2):c.591+1G>C	rs200610775	0.00016
NM_006440.5(TXNRD2):c.1036C>T (p.Arg346Trp)	rs61736941	0.00014
NM_006440.5(TXNRD2):c.745C>T (p.Arg249Cys)	rs557142042	0.00009
NM_006440.5(TXNRD2):c.1030G>T (p.Asp344Tyr)	rs373839226	0.00008
NM_006440.5(TXNRD2):c.175G>A (p.Ala59Thr)	rs752863555	0.00007
NM_006440.5(TXNRD2):c.1348-2A>G	rs768600057	0.00005
NM_006440.5(TXNRD2):c.139G>A (p.Gly47Arg)	rs759298418	0.00004
NM_006440.5(TXNRD2):c.760C>T (p.Arg254Cys)	rs183950022	0.00004
NM_006440.5(TXNRD2):c.1037G>A (p.Arg346Gln)	rs201349663	0.00003
NM_006440.5(TXNRD2):c.529A>G (p.Ile177Val)	rs373970291	0.00001
NM_006440.5(TXNRD2):c.1370dup (p.Gln458fs)	rs758790391
NM_006440.5(TXNRD2):c.392C>T (p.Ala131Val)	rs368359642
NM_006440.5(TXNRD2):c.41_42delinsTT (p.Arg14Leu)	rs2146120283

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