List of variants in gene RAD52 reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_134424.4(RAD52):c.*395G>A	rs104895058	0.00667
NM_134424.4(RAD52):c.186+89C>T	rs104895071	0.00628
NM_134424.4(RAD52):c.467+21C>T	rs104895070	0.00397
NM_134424.4(RAD52):c.467+86A>G	rs104895069	0.00163
NM_134424.4(RAD52):c.*453C>T	rs104895057	0.00126
NM_134424.4(RAD52):c.*468C>T	rs104895056	0.00071
NM_134424.4(RAD52):c.*317G>A	rs104895065	0.00002
NM_134424.4(RAD52):c.*1194C>T	rs104895054
NM_134424.4(RAD52):c.*315T>A	rs104895067
NM_134424.4(RAD52):c.*316G>C	rs104895066
NM_134424.4(RAD52):c.*318C>A	rs104895064
NM_134424.4(RAD52):c.*320C>A	rs104895063
NM_134424.4(RAD52):c.*321C>A	rs104895062
NM_134424.4(RAD52):c.*322T>A	rs104895061
NM_134424.4(RAD52):c.*324G>A	rs104895060
NM_134424.4(RAD52):c.*325C>G	rs104895059
NM_134424.4(RAD52):c.*992T>G	rs104895055

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