List of variants in gene combination FANCM, LOC130055524 reported as likely benign for immune system 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: 9

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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.93A>G (p.Arg31=)	rs112641528	0.00007
NM_020937.4(FANCM):c.59C>G (p.Ser20Cys)	rs199699785	0.00006
NM_020937.4(FANCM):c.63G>C (p.Gly21=)	rs563248675	0.00002
NM_020937.4(FANCM):c.54A>G (p.Arg18=)	rs1885467009
NM_020937.4(FANCM):c.69G>C (p.Pro23=)
NM_020937.4(FANCM):c.75C>T (p.Cys25=)	rs1885469049
NM_020937.4(FANCM):c.78C>T (p.Ser26=)
NM_020937.4(FANCM):c.81C>T (p.Ser27=)	rs1388168603

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