ClinVar Miner

List of variants in gene MORC2 reported as uncertain significance for Inborn genetic diseases

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_001303256.3(MORC2):c.712C>T (p.Arg238Cys) rs371713427 0.00010
NM_001303256.3(MORC2):c.2668G>A (p.Glu890Lys) rs201090445 0.00006
NM_001303256.3(MORC2):c.2677C>T (p.Arg893Cys) rs150496681 0.00006
NM_001303256.3(MORC2):c.1451G>A (p.Arg484His) rs143046507 0.00004
NM_001303256.3(MORC2):c.1949C>T (p.Thr650Ile) rs371710965 0.00004
NM_001303256.3(MORC2):c.1823G>A (p.Arg608His) rs781443418 0.00003
NM_001303256.3(MORC2):c.2106C>A (p.Asn702Lys) rs201032497 0.00003
NM_001303256.3(MORC2):c.2634G>C (p.Gln878His) rs1388475410 0.00003
NM_001303256.3(MORC2):c.2243T>C (p.Val748Ala) rs746418433 0.00002
NM_001303256.3(MORC2):c.683C>T (p.Thr228Met) rs774960940 0.00002
NM_001303256.3(MORC2):c.839C>T (p.Thr280Met) rs764379949 0.00002
NM_001303256.3(MORC2):c.1369+5T>A rs147800268 0.00001
NM_001303256.3(MORC2):c.1370-3C>T rs770913783 0.00001
NM_001303256.3(MORC2):c.1603C>T (p.Arg535Trp) rs576981610 0.00001
NM_001303256.3(MORC2):c.1604G>A (p.Arg535Gln) rs750003469 0.00001
NM_001303256.3(MORC2):c.1705C>T (p.Arg569Cys) rs267606222 0.00001
NM_001303256.3(MORC2):c.1925G>A (p.Arg642Gln) rs765892287 0.00001
NM_001303256.3(MORC2):c.1942A>G (p.Ser648Gly) rs200703581 0.00001
NM_001303256.3(MORC2):c.227-5T>C rs763643471 0.00001
NM_001303256.3(MORC2):c.2411A>G (p.Asn804Ser) rs759734334 0.00001
NM_001303256.3(MORC2):c.2725G>A (p.Asp909Asn) rs770586964 0.00001
NM_001303256.3(MORC2):c.2880C>G (p.Asn960Lys) rs750335952 0.00001
NM_001303256.3(MORC2):c.2888A>G (p.Asn963Ser) rs781162787 0.00001
NM_001303256.3(MORC2):c.2963G>A (p.Arg988His) rs747693260 0.00001
NM_001303256.3(MORC2):c.3031-4C>G rs373542143 0.00001
NM_001303256.3(MORC2):c.470C>G (p.Pro157Arg) rs370868047 0.00001
NM_001303256.3(MORC2):c.825-3C>A rs752040112 0.00001
NM_001303256.3(MORC2):c.1129C>T (p.Arg377Trp)
NM_001303256.3(MORC2):c.1181A>G (p.Tyr394Cys) rs1555938796
NM_001303256.3(MORC2):c.1199A>G (p.Gln400Arg)
NM_001303256.3(MORC2):c.122+4T>C
NM_001303256.3(MORC2):c.1265A>G (p.Glu422Gly) rs2040680054
NM_001303256.3(MORC2):c.1343C>T (p.Ala448Val)
NM_001303256.3(MORC2):c.1421A>G (p.Asn474Ser)
NM_001303256.3(MORC2):c.1813-3dup
NM_001303256.3(MORC2):c.1939A>G (p.Ile647Val)
NM_001303256.3(MORC2):c.1976G>A (p.Arg659Gln) rs769791429
NM_001303256.3(MORC2):c.2125G>A (p.Val709Ile)
NM_001303256.3(MORC2):c.217A>G (p.Met73Val)
NM_001303256.3(MORC2):c.2221G>A (p.Ala741Thr)
NM_001303256.3(MORC2):c.2346A>C (p.Glu782Asp) rs751495570
NM_001303256.3(MORC2):c.2405G>T (p.Arg802Leu)
NM_001303256.3(MORC2):c.2548C>T (p.Arg850Trp)
NM_001303256.3(MORC2):c.2585_2603dup (p.Gly868_Gly869insTer) rs1555936598
NM_001303256.3(MORC2):c.2839C>G (p.Leu947Val)
NM_001303256.3(MORC2):c.489G>C (p.Glu163Asp)
NM_001303256.3(MORC2):c.68+4A>C
NM_001303256.3(MORC2):c.802T>C (p.Ser268Pro) rs2040740411
NM_001303256.3(MORC2):c.859C>T (p.Arg287Cys)
NM_001303256.3(MORC2):c.892G>C (p.Val298Leu) rs772766261
NM_001303256.3(MORC2):c.905-24_905-5dup
NM_001303256.3(MORC2):c.988G>A (p.Val330Met) rs1390155636

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