ClinVar Miner

List of variants in gene MYL3 reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_000258.3(MYL3):c.307+37A>C rs2227294 0.34149
NM_000258.3(MYL3):c.129+44G>T rs936175 0.30333
NM_000258.3(MYL3):c.*89G>A rs1042973 0.17840
NM_000258.3(MYL3):c.69C>T (p.Pro23=) rs2233264 0.02058
NM_000258.3(MYL3):c.130-14G>T rs192329378 0.00198
NM_000258.3(MYL3):c.81T>C (p.Pro27=) rs147584015 0.00133
NM_000258.3(MYL3):c.559+6C>T rs199474709 0.00077
NM_000258.3(MYL3):c.482-14C>A rs201780962 0.00048
NM_000258.3(MYL3):c.157+8G>C rs777555567 0.00013
NM_000258.3(MYL3):c.559+19G>A rs552393482 0.00012
NM_000258.3(MYL3):c.*5C>T rs727505197 0.00004
NM_000258.3(MYL3):c.92G>A (p.Arg31His) rs199639940 0.00003
NM_000258.3(MYL3):c.*3C>T rs748154150 0.00002
NM_000258.3(MYL3):c.286C>T (p.Leu96=) rs772804040 0.00002
NM_000258.3(MYL3):c.532G>A (p.Asp178Asn) rs145520567 0.00002
NM_000258.3(MYL3):c.261C>T (p.Pro87=) rs556711370
NM_000258.3(MYL3):c.411G>A (p.Leu137=) rs2233265
NM_000258.3(MYL3):c.411G>T (p.Leu137=) rs2233265

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