List of variants in gene PALB2 reported as not provided for hematologic disorder

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.298C>T (p.Leu100Phe)	rs61756147	0.00021
NM_024675.4(PALB2):c.2674G>A (p.Glu892Lys)	rs45476495	0.00004
NM_024675.4(PALB2):c.3113G>A (p.Trp1038Ter)	rs180177132	0.00002
NM_024675.4(PALB2):c.1616_1617dup (p.Asn540fs)	rs786203346	0.00001
NM_024675.4(PALB2):c.2386G>T (p.Gly796Ter)	rs180177112	0.00001
GRCh37/hg19 16p12.2(chr16:23614483-23619333)x1
NM_024675.4(PALB2):c.1490del (p.Asn497fs)	rs1555461253
NM_024675.4(PALB2):c.2368C>T (p.Gln790Ter)	rs886039480
NM_024675.4(PALB2):c.2571G>A (p.Leu857=)	rs587780821
NM_024675.4(PALB2):c.757_758del (p.Leu253fs)	rs180177092

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