ClinVar Miner

List of variants reported as benign for Fanconi anemia complementation group U

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.563G>A (p.Arg188His) rs3218536 0.04933
NM_005431.2(XRCC2):c.40-10C>T rs3218472 0.01055
NM_005431.2(XRCC2):c.40-16T>C rs41274991 0.00141
NM_005431.2(XRCC2):c.300A>G (p.Leu100=) rs146700851 0.00001

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