List of variants in gene PALB2 reported as uncertain significance by GeneKor MSA

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp)	rs183489969	0.00016
NM_024675.4(PALB2):c.1544A>G (p.Lys515Arg)	rs515726072	0.00009
NM_024675.4(PALB2):c.3508C>T (p.His1170Tyr)	rs200283306	0.00009
NM_024675.4(PALB2):c.3296C>G (p.Thr1099Arg)	rs142132127	0.00003
NM_024675.4(PALB2):c.1123C>A (p.Leu375Ile)	rs373298267	0.00001
NM_024675.4(PALB2):c.1448C>T (p.Ser483Leu)	rs1057520736	0.00001
NM_024675.4(PALB2):c.2792T>G (p.Leu931Arg)	rs773831304	0.00001
NM_024675.4(PALB2):c.292A>G (p.Ile98Val)	rs587782831	0.00001
NM_024675.4(PALB2):c.3073G>A (p.Ala1025Thr)	rs746872839	0.00001
NM_024675.4(PALB2):c.3320T>C (p.Leu1107Pro)	rs149194681	0.00001
NM_024675.4(PALB2):c.739A>G (p.Thr247Ala)	rs786203040	0.00001
NM_024675.4(PALB2):c.1152A>G (p.Glu384=)	rs1567221490
NM_024675.4(PALB2):c.1537A>C (p.Thr513Pro)	rs1060502741
NM_024675.4(PALB2):c.2461A>T (p.Asn821Tyr)	rs958566673
NM_024675.4(PALB2):c.2813A>G (p.Asn938Ser)	rs1567214357
NM_024675.4(PALB2):c.3122A>C (p.Lys1041Thr)	rs781663559
NM_024675.4(PALB2):c.3306C>G (p.Ser1102Arg)	rs515726112
NM_024675.4(PALB2):c.833_834delinsAT (p.Leu278His)	rs587778582

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