List of variants in gene PRDM8 reported as benign by Invitae

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001099403.2(PRDM8):c.1980G>C (p.Arg660=)	rs12780	0.26373
NM_001099403.2(PRDM8):c.762C>T (p.Ser254=)	rs142234659	0.05105
NM_001099403.2(PRDM8):c.1726C>T (p.Leu576=)	rs28405693	0.04102
NM_001099403.2(PRDM8):c.1683C>T (p.Ser561=)	rs150632206	0.01930
NM_001099403.2(PRDM8):c.1447G>T (p.Ala483Ser)	rs544862921	0.00503
NM_001099403.2(PRDM8):c.722C>A (p.Pro241Gln)	rs200010979	0.00497
NM_001099403.2(PRDM8):c.1137C>A (p.Gly379=)	rs144810863	0.00461
NM_001099403.2(PRDM8):c.1050C>T (p.Cys350=)	rs374280707	0.00420
NM_001099403.2(PRDM8):c.1390C>T (p.Pro464Ser)	rs201251555	0.00402
NM_001099403.2(PRDM8):c.1011A>C (p.Val337=)	rs755114294	0.00142
NM_001099403.2(PRDM8):c.1857G>T (p.Leu619=)	rs140737026	0.00121
NM_001099403.2(PRDM8):c.117T>C (p.Ala39=)	rs369098269	0.00025
NM_001099403.2(PRDM8):c.1778_1795del (p.Ala593_Ala598del)	rs755316101

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