ClinVar Miner

Variants in gene MYL3 with conflicting interpretations "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: 11
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HGVS dbSNP
NM_000258.2(MYL3):c.130-14G>T rs192329378
NM_000258.2(MYL3):c.157+8G>C rs777555567
NM_000258.2(MYL3):c.261C>T (p.Pro87=) rs556711370
NM_000258.2(MYL3):c.286C>T (p.Leu96=) rs772804040
NM_000258.2(MYL3):c.307+15C>T rs184025552
NM_000258.2(MYL3):c.411G>T (p.Leu137=) rs2233265
NM_000258.2(MYL3):c.477G>T (p.Thr159=) rs148365503
NM_000258.2(MYL3):c.482-14C>A rs201780962
NM_000258.2(MYL3):c.559+6C>T rs199474709
NM_000258.2(MYL3):c.69C>T (p.Pro23=) rs2233264
NM_000258.2(MYL3):c.81T>C (p.Pro27=) rs147584015

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