List of variants in gene PALB2 reported as likely benign by Mendelics

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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: 28

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.2794G>A (p.Val932Met)	rs45624036	0.00449
NM_024675.4(PALB2):c.2590C>T (p.Pro864Ser)	rs45568339	0.00287
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.1470C>T (p.Pro490=)	rs45612837	0.00035
NM_024675.4(PALB2):c.656A>G (p.Asp219Gly)	rs45594034	0.00021
NM_024675.4(PALB2):c.2135C>T (p.Ala712Val)	rs141458731	0.00017
NM_024675.4(PALB2):c.2509G>A (p.Glu837Lys)	rs587778587	0.00008
NM_024675.4(PALB2):c.1935G>A (p.Glu645=)	rs141707455	0.00006
NM_024675.4(PALB2):c.560C>A (p.Pro187His)	rs371582757	0.00006
NM_024675.4(PALB2):c.768C>T (p.Ser256=)	rs45487491	0.00006
NM_024675.4(PALB2):c.1311A>G (p.Lys437=)	rs190489275	0.00001
NM_024675.4(PALB2):c.1611G>A (p.Ser537=)	rs730881874	0.00001
NM_024675.4(PALB2):c.1923A>G (p.Lys641=)	rs775283927	0.00001
NM_024675.4(PALB2):c.212-6C>T	rs1416424510	0.00001
NM_024675.4(PALB2):c.495C>T (p.Gly165=)	rs200937538	0.00001
NM_024675.4(PALB2):c.-23C>T	rs1597106322
NM_024675.4(PALB2):c.-66C>T	rs1597106467
NM_024675.4(PALB2):c.1089T>C (p.Asp363=)	rs1597097155
NM_024675.4(PALB2):c.1226A>G (p.Tyr409Cys)	rs878855097
NM_024675.4(PALB2):c.1685-28T>C	rs1597091553
NM_024675.4(PALB2):c.1917G>T (p.Glu639Asp)	rs1597090787
NM_024675.4(PALB2):c.212-50dup	rs759760268
NM_024675.4(PALB2):c.212-8C>T	rs1387711045
NM_024675.4(PALB2):c.212-9C>T	rs1555461884
NM_024675.4(PALB2):c.2961A>G (p.Gln987=)	rs1555459530
NM_024675.4(PALB2):c.2996+9del	rs769414858
NM_024675.4(PALB2):c.49-432A>G	rs1597102250

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