List of variants in gene PALB2 reported by True Health Diagnostics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.3300T>G (p.Thr1100=)	rs45516100	0.02529
NM_024675.4(PALB2):c.2014G>C (p.Glu672Gln)	rs45532440	0.02171
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.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.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.298C>T (p.Leu100Phe)	rs61756147	0.00021
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.2027T>C (p.Ile676Thr)	rs200875161	0.00011
NM_024675.4(PALB2):c.1623G>A (p.Arg541=)	rs745665968	0.00009
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.1699C>T (p.His567Tyr)	rs370422990	0.00004
NM_024675.4(PALB2):c.2289G>C (p.Leu763Phe)	rs373478248	0.00004
NM_024675.4(PALB2):c.196C>T (p.Gln66Ter)	rs180177083	0.00001
NM_024675.4(PALB2):c.2478C>T (p.Asn826=)	rs786201885	0.00001
NM_024675.4(PALB2):c.315G>C (p.Glu105Asp)	rs515726108	0.00001
NM_024675.4(PALB2):c.2752C>T (p.Pro918Ser)	rs515726094
NM_024675.4(PALB2):c.991G>C (p.Glu331Gln)	rs878855126

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