ClinVar Miner

List of variants reported as benign for Fanconi anemia by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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NM_000059.4(BRCA2):c.2229T>C (p.His743=) rs1801499
NM_007294.4(BRCA1):c.2311T>C (p.Leu771=) rs16940
NM_007294.4(BRCA1):c.3113A>G (p.Glu1038Gly) rs16941

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