ClinVar Miner

List of variants in gene MYH11 reported as uncertain significance for congenital anomaly of the great arteries

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_002474.3(MYH11):c.3560C>T (p.Thr1187Met) rs552818350
NM_002474.3(MYH11):c.3728T>C (p.Leu1243Pro) rs1555554139

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