ClinVar Miner

List of variants in gene combination ATP6V0A2, TCTN2 reported as benign for Meckel syndrome, type 1

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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NM_024809.5(TCTN2):c.*330_*331insACTC rs56918215
NM_024809.5(TCTN2):c.2041T>C (p.Leu681=) rs112158562

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