List of variants in gene PALB2 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.2816T>G (p.Leu939Trp)	rs45478192	0.00121
NM_024675.4(PALB2):c.1194G>A (p.Val398=)	rs61755173	0.00103
NM_024675.4(PALB2):c.2851T>C (p.Ser951Pro)	rs149522412	0.00058
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp)	rs183489969	0.00016
NM_024675.4(PALB2):c.2027T>C (p.Ile676Thr)	rs200875161	0.00011
NM_024675.4(PALB2):c.12T>C (p.Pro4=)	rs567706422	0.00009
NM_024675.4(PALB2):c.3249G>C (p.Glu1083Asp)	rs147045425	0.00005
NM_024675.4(PALB2):c.1316G>T (p.Gly439Val)	rs537258442	0.00004
NM_024675.4(PALB2):c.1540G>A (p.Gly514Arg)	rs756778249	0.00001
NM_024675.4(PALB2):c.1792C>T (p.Leu598=)	rs746702349	0.00001
NM_024675.4(PALB2):c.2438T>C (p.Ile813Thr)	rs763191051	0.00001
NM_024675.4(PALB2):c.3483T>C (p.Phe1161=)	rs372686500	0.00001
NM_024675.4(PALB2):c.212-10del	rs766487430
NM_024675.4(PALB2):c.9G>A (p.Glu3=)	rs786202325

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