ClinVar Miner

List of variants reported as uncertain significance for FG syndrome by Laboratoire de Cytogenetique,Hospices Civils de Lyon

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_001110556.2(FLNA):c.7628G>A (p.Cys2543Tyr) rs201762017
NM_005120.3(MED12):c.2023C>T (p.Leu675Phe) rs1307587368
NM_005120.3(MED12):c.5017_5019AAG[1] (p.Lys1674del)

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