ClinVar Miner

List of variants in gene combination FANCL, VRK2 reported as benign for bone development disease

Included ClinVar conditions (614):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_018062.4(FANCL):c.*95A>G rs76348639 0.00754
NM_006296.7(VRK2):c.*102_*105dup rs759217526

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