ClinVar Miner

List of variants in gene RAB3GAP2 reported as likely benign for Warburg micro syndrome 2

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_012414.4(RAB3GAP2):c.1215C>T (p.Phe405=) rs762485949
NM_012414.4(RAB3GAP2):c.2168T>A (p.Val723Glu) rs150643803
NM_012414.4(RAB3GAP2):c.2417-7C>T rs973067244
NM_012414.4(RAB3GAP2):c.2667T>G (p.Leu889=) rs145550355
NM_012414.4(RAB3GAP2):c.4060A>G (p.Ile1354Val) rs59190330
NM_012414.4(RAB3GAP2):c.4161C>T (p.Ala1387=) rs772430156
NM_012414.4(RAB3GAP2):c.812-6T>A rs575925720

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