ClinVar Miner

Variants in gene RAG2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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NM_000536.4(RAG2):c.*52T>A rs546979744
NM_000536.4(RAG2):c.1391G>A (p.Arg464His) rs147748696
NM_000536.4(RAG2):c.1504A>G (p.Met502Val) rs145614809
NM_000536.4(RAG2):c.63G>A (p.Leu21=) rs142797325
NM_000536.4(RAG2):c.644C>T (p.Thr215Ile) rs35691292

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