List of variants in gene FANCM reported as benign for anemia

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: 45

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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.3758A>G (p.Asn1253Ser)	rs45604036	0.02192
NM_020937.4(FANCM):c.5627A>G (p.Asn1876Ser)	rs45557033	0.02173
NM_020937.4(FANCM):c.229A>G (p.Thr77Ala)	rs61746895	0.01981
NM_020937.4(FANCM):c.4799C>T (p.Thr1600Ile)	rs61746943	0.01614
NM_020937.4(FANCM):c.1964A>G (p.Asn655Ser)	rs61753893	0.01090
NM_020937.4(FANCM):c.624A>G (p.Ile208Met)	rs45547534	0.01077
NM_020937.4(FANCM):c.5190G>A (p.Gln1730=)	rs7142192	0.00916
NM_020937.4(FANCM):c.3863A>G (p.Asn1288Ser)	rs116519044	0.00914
NM_020937.4(FANCM):c.5656C>T (p.His1886Tyr)	rs79343837	0.00864
NM_020937.4(FANCM):c.5142G>A (p.Ala1714=)	rs111894696	0.00835
NM_020937.4(FANCM):c.5224A>G (p.Ile1742Val)	rs143662421	0.00824
NM_020937.4(FANCM):c.2445G>A (p.Ser815=)	rs61745871	0.00791
NM_020937.4(FANCM):c.3920A>G (p.Tyr1307Cys)	rs61730251	0.00456
NM_020937.4(FANCM):c.3040G>T (p.Gly1014Cys)	rs77532752	0.00398
NM_020937.4(FANCM):c.4563A>C (p.Glu1521Asp)	rs113986680	0.00382
NM_020937.4(FANCM):c.527C>T (p.Thr176Ile)	rs77374493	0.00371
NM_020937.4(FANCM):c.2190A>G (p.Gln730=)	rs117392855	0.00320
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.5577T>C (p.Asn1859=)	rs113831595	0.00300
NM_020937.4(FANCM):c.2749A>G (p.Ile917Val)	rs148871932	0.00268
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.1041G>A (p.Pro347=)	rs140998495	0.00147
NM_020937.4(FANCM):c.1397-12A>G	rs560956489	0.00092
NM_020937.4(FANCM):c.990A>G (p.Thr330=)	rs138677111	0.00066
NM_020937.4(FANCM):c.4931G>A (p.Arg1644Gln)	rs138151018	0.00046
NM_020937.4(FANCM):c.30G>A (p.Gln10=)	rs145745979	0.00014
NM_020937.4(FANCM):c.4222+18dup	rs760075544	0.00008
NM_020937.4(FANCM):c.1183+8A>G	rs538172189	0.00001
NM_020937.4(FANCM):c.1397-15TA[6]	rs112326758
NM_020937.4(FANCM):c.1397-15TA[8]	rs112326758
NM_020937.4(FANCM):c.4387-16del
NM_020937.4(FANCM):c.4515+14del	rs747887646
NM_020937.4(FANCM):c.4516-5_4516-2del	rs796584585
NM_020937.4(FANCM):c.682-7del	rs759364320
NM_020937.4(FANCM):c.682-7dup	rs759364320
NM_020937.4(FANCM):c.876G>T (p.Pro292=)	rs150757891

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