ClinVar Miner

List of variants in gene combination FANCI, POLG reported as benign for Fanconi anemia complementation group A

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_001113378.1(FANCI):c.3906T>C (p.Gly1302=) rs1138465
NM_002693.2(POLG):c.*49dup rs3087377
NM_002693.2(POLG):c.3105-11T>C rs2302084
NM_002693.2(POLG):c.3643+257T>G rs1061316
NM_002693.2(POLG):c.3643+258A>G rs1860021

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