ClinVar Miner

Variants in gene combination LOC101927870, RELN with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 12
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HGVS dbSNP
NM_005045.4(RELN):c.10074A>G (p.Ala3358=) rs1062831
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile) rs115035120
NM_005045.4(RELN):c.10182-11G>A rs57844600
NM_005045.4(RELN):c.8120-9T>C rs74952625
NM_005045.4(RELN):c.8136A>G (p.Leu2712=) rs3808039
NM_005045.4(RELN):c.8508C>T (p.Phe2836=) rs2229862
NM_005045.4(RELN):c.8811G>A (p.Ala2937=) rs144728023
NM_005045.4(RELN):c.8843+7G>C rs2711885
NM_005045.4(RELN):c.9524A>C (p.His3175Pro) rs74513461
NM_005045.4(RELN):c.9714C>T (p.His3238=) rs78218774
NM_005045.4(RELN):c.9730G>A (p.Gly3244Ser) rs73714410
NM_005045.4(RELN):c.9903C>T (p.Tyr3301=) rs73714404

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