List of variants in gene FANCM reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.2632G>T (p.Val878Leu)	rs1367580	0.19378
NM_020937.4(FANCM):c.524C>T (p.Ser175Phe)	rs10138997	0.16789
NM_020937.4(FANCM):c.5434C>G (p.Pro1812Ala)	rs3736772	0.08766
NM_020937.4(FANCM):c.4378A>G (p.Ile1460Val)	rs78211950	0.08024
NM_020937.4(FANCM):c.2670T>C (p.Phe890=)	rs8017226	0.03114
NM_020937.4(FANCM):c.6141T>C (p.Asp2047=)	rs8018014	0.03012
NM_020937.4(FANCM):c.624A>G (p.Ile208Met)	rs45547534	0.01077
NM_020937.4(FANCM):c.4516-5_4516-2del	rs796584585

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