List of variants in gene combination FANCM, LOC130055524 studied for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.53G>A (p.Arg18Gln)	rs146609069	0.00011
NM_020937.4(FANCM):c.59C>G (p.Ser20Cys)	rs199699785	0.00006
NM_020937.4(FANCM):c.56C>T (p.Ser19Leu)	rs201383385	0.00003
NM_020937.4(FANCM):c.68C>A (p.Pro23Gln)	rs377031191	0.00003
NM_020937.4(FANCM):c.92G>T (p.Arg31Leu)	rs886050496	0.00002
NM_020937.4(FANCM):c.100_117del (p.Ser34_Lys39del)	rs1885472531
NM_020937.4(FANCM):c.53G>C (p.Arg18Pro)
NM_020937.4(FANCM):c.77G>A (p.Ser26Asn)

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