ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP gnomAD frequency
NM_001032386.2(SUOX):c.574C>T (p.Arg192Trp) rs139444405 0.00017
NM_001032386.2(SUOX):c.50+9G>A rs368327991 0.00006
NM_001032386.2(SUOX):c.1137A>G (p.Lys379=) rs759992645 0.00003
NM_001032386.2(SUOX):c.192C>T (p.Leu64=) rs577360771 0.00002
NM_001032386.2(SUOX):c.279C>T (p.His93=) rs763253683 0.00001
NM_001032386.2(SUOX):c.507C>T (p.Thr169=) rs765012855 0.00001
NM_001032386.2(SUOX):c.1636T>A (p.Ter546Arg) rs574353697

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