ClinVar Miner

List of variants in gene FANCM reported as likely benign for anemia (disease)

Included ClinVar conditions (263):
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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_020937.4(FANCM):c.*232G>A rs7155480
NM_020937.4(FANCM):c.1040C>T (p.Pro347Leu) rs151071546
NM_020937.4(FANCM):c.1041G>A (p.Pro347=) rs140998495
NM_020937.4(FANCM):c.1396+10A>G rs371211104
NM_020937.4(FANCM):c.1397-15TA[6] rs112326758
NM_020937.4(FANCM):c.171G>C (p.Leu57Phe) rs142007602
NM_020937.4(FANCM):c.2190A>G (p.Gln730=) rs117392855
NM_020937.4(FANCM):c.219C>A (p.Gly73=) rs111252426
NM_020937.4(FANCM):c.2267G>A (p.Arg756His) rs142763060
NM_020937.4(FANCM):c.2268C>A (p.Arg756=) rs146061601
NM_020937.4(FANCM):c.229A>G (p.Thr77Ala) rs61746895
NM_020937.4(FANCM):c.231C>T (p.Thr77=) rs377164876
NM_020937.4(FANCM):c.2330A>G (p.Tyr777Cys) rs200173413
NM_020937.4(FANCM):c.2445G>A (p.Ser815=) rs61745871
NM_020937.4(FANCM):c.2628T>C (p.Asp876=) rs374313777
NM_020937.4(FANCM):c.2670T>C (p.Phe890=) rs8017226
NM_020937.4(FANCM):c.2703A>G (p.Ser901=) rs781066677
NM_020937.4(FANCM):c.2749A>G (p.Ile917Val) rs148871932
NM_020937.4(FANCM):c.2889C>T (p.Phe963=) rs544323144
NM_020937.4(FANCM):c.3296G>A (p.Arg1099His) rs139382267
NM_020937.4(FANCM):c.3758A>G (p.Asn1253Ser) rs45604036
NM_020937.4(FANCM):c.4311T>C (p.Ser1437=) rs1017827085
NM_020937.4(FANCM):c.4378A>G (p.Ile1460Val) rs78211950
NM_020937.4(FANCM):c.4709G>A (p.Arg1570His) rs201803784
NM_020937.4(FANCM):c.4799C>T (p.Thr1600Ile) rs61746943
NM_020937.4(FANCM):c.491A>C (p.His164Pro) rs144278051
NM_020937.4(FANCM):c.5022T>C (p.Ser1674=) rs1295913364
NM_020937.4(FANCM):c.5026G>A (p.Glu1676Lys) rs769919966
NM_020937.4(FANCM):c.5142G>A (p.Ala1714=) rs111894696
NM_020937.4(FANCM):c.5199G>A (p.Gln1733=) rs1555367253
NM_020937.4(FANCM):c.523T>C (p.Ser175Pro) rs779858649
NM_020937.4(FANCM):c.5434C>G (p.Pro1812Ala) rs3736772
NM_020937.4(FANCM):c.5627A>G (p.Asn1876Ser) rs45557033
NM_020937.4(FANCM):c.5685T>C (p.Cys1895=) rs746870942
NM_020937.4(FANCM):c.6084T>C (p.Tyr2028=) rs756119280
NM_020937.4(FANCM):c.6141T>C (p.Asp2047=) rs8018014
NM_020937.4(FANCM):c.693A>G (p.Glu231=) rs146597866
NM_020937.4(FANCM):c.926A>C (p.Glu309Ala) rs143006771

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