List of variants in gene PALB2 reported as likely benign by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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_024675.4(PALB2):c.629C>T (p.Pro210Leu)	rs57605939	0.02101
NM_024675.4(PALB2):c.2993G>A (p.Gly998Glu)	rs45551636	0.01717
NM_024675.4(PALB2):c.1010T>C (p.Leu337Ser)	rs45494092	0.01508
NM_024675.4(PALB2):c.925A>G (p.Ile309Val)	rs3809683	0.00919
NM_024675.4(PALB2):c.53A>G (p.Lys18Arg)	rs138789658	0.00530
NM_024675.4(PALB2):c.2794G>A (p.Val932Met)	rs45624036	0.00449
NM_024675.4(PALB2):c.1572A>G (p.Ser524=)	rs45472400	0.00312
NM_024675.4(PALB2):c.1419A>C (p.Pro473=)	rs62625275	0.00309
NM_024675.4(PALB2):c.2256A>G (p.Gly752=)	rs147120218	0.00193
NM_024675.4(PALB2):c.2742C>T (p.Phe914=)	rs115759702	0.00143
NM_024675.4(PALB2):c.2135C>T (p.Ala712Val)	rs141458731	0.00017
NM_024675.4(PALB2):c.1699C>T (p.His567Tyr)	rs370422990	0.00004
NM_024675.4(PALB2):c.2082A>G (p.Thr694=)	rs781440401	0.00004
NM_024675.4(PALB2):c.833T>A (p.Leu278Gln)	rs200843485	0.00001
NM_024675.4(PALB2):c.834A>T (p.Leu278=)	rs199919863	0.00001
NM_024675.4(PALB2):c.1881G>T (p.Val627=)	rs139362268
NM_024675.4(PALB2):c.212-10del	rs766487430

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