List of variants in gene FANCM reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.3547T>C (p.Leu1183=)	rs142667852	0.00318
NM_020937.4(FANCM):c.4222+7T>G	rs148675704	0.00316
NM_020937.4(FANCM):c.4260C>T (p.Asp1420=)	rs113819179	0.00254
NM_020937.4(FANCM):c.1040C>T (p.Pro347Leu)	rs151071546	0.00243
NM_020937.4(FANCM):c.5808C>T (p.Ser1936=)	rs142333130	0.00178
NM_020937.4(FANCM):c.2268C>A (p.Arg756=)	rs146061601	0.00128
NM_020937.4(FANCM):c.4147T>G (p.Tyr1383Asp)	rs144104545	0.00118
NM_020937.4(FANCM):c.3296G>A (p.Arg1099His)	rs139382267	0.00083
NM_020937.4(FANCM):c.3681A>G (p.Leu1227=)	rs61749475	0.00047
NM_020937.4(FANCM):c.4931G>A (p.Arg1644Gln)	rs138151018	0.00046
NM_020937.4(FANCM):c.1812C>T (p.Asn604=)	rs377473850	0.00011
NM_020937.4(FANCM):c.1752G>A (p.Arg584=)	rs373696744	0.00004
NM_020937.4(FANCM):c.4878T>C (p.Asp1626=)	rs150389713	0.00003
NM_020937.4(FANCM):c.5208G>A (p.Leu1736=)	rs746368298	0.00002
NM_020937.4(FANCM):c.117G>A (p.Lys39=)	rs765275634	0.00001
NM_020937.4(FANCM):c.366C>G (p.Ala122=)	rs770311755	0.00001
NM_020937.4(FANCM):c.5717-4T>A	rs781258517	0.00001

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