List of variants in gene PALB2 reported as uncertain significance for embryonal neoplasm

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.1042C>A (p.Gln348Lys)	rs375699023	0.00008
NM_024675.4(PALB2):c.2755G>A (p.Val919Ile)	rs775193384	0.00002
NM_024675.4(PALB2):c.3103A>G (p.Ile1035Val)	rs863224783	0.00001
NM_024675.4(PALB2):c.3494C>T (p.Ser1165Leu)	rs773829275	0.00001
NM_024675.4(PALB2):c.1600T>G (p.Ser534Ala)	rs1064793824
NM_024675.4(PALB2):c.398G>C (p.Ser133Thr)	rs864622411

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