List of variants in gene MORC2 reported by Ambry Genetics

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: 66

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HGVS	dbSNP	gnomAD frequency
NM_001303256.3(MORC2):c.2747+5_2747+6del	rs67357185	0.00339
NM_001303256.3(MORC2):c.2044G>A (p.Val682Ile)	rs144493873	0.00061
NM_001303256.3(MORC2):c.1754G>A (p.Arg585His)	rs137983239	0.00019
NM_001303256.3(MORC2):c.969C>A (p.Asp323Glu)	rs199973357	0.00019
NM_001303256.3(MORC2):c.489G>T (p.Glu163Asp)	rs186458188	0.00017
NM_001303256.3(MORC2):c.2066C>T (p.Ala689Val)	rs560948457	0.00013
NM_001303256.3(MORC2):c.712C>T (p.Arg238Cys)	rs371713427	0.00010
NM_001303256.3(MORC2):c.258G>C (p.Lys86Asn)	rs150980372	0.00006
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.2354C>T (p.Ser785Leu)	rs551185965	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.2270A>G (p.Glu757Gly)	rs774444542	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.518A>C (p.Tyr173Ser)	rs144248516	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.1822C>T (p.Arg608Cys)	rs373963382
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.260C>T (p.Ser87Leu)	rs864309504
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.754C>T (p.Arg252Trp)	rs864309503
NM_001303256.3(MORC2):c.79G>A (p.Glu27Lys)	rs1602510200
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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