ClinVar Miner

Variants in gene SUOX with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP gnomAD frequency
NM_001032386.2(SUOX):c.1358G>A (p.Gly453Asp) rs76537761 0.00392
NM_001032386.2(SUOX):c.629C>T (p.Pro210Leu) rs141735896 0.00351
NM_001032386.2(SUOX):c.119G>A (p.Arg40His) rs117778870 0.00049
NM_001032386.2(SUOX):c.1050T>C (p.Tyr350=) rs184819190 0.00027
NM_001032386.2(SUOX):c.1281G>C (p.Ser427=) rs773115

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