List of variants in gene MCM4 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_182746.3(MCM4):c.*1305del	rs17334556	0.04078
NM_182746.3(MCM4):c.2064G>A (p.Lys688=)	rs143488457	0.00503
NM_182746.3(MCM4):c.1659A>G (p.Thr553=)	rs17287677	0.00313
NM_182746.3(MCM4):c.-65A>T	rs552020479	0.00211
NM_182746.3(MCM4):c.1406G>C (p.Ser469Thr)	rs117063344	0.00202
NM_182746.3(MCM4):c.833-14T>C	rs191317744	0.00131
NM_182746.3(MCM4):c.1569G>A (p.Val523=)	rs765660789	0.00109
NM_182746.3(MCM4):c.*871G>A	rs192670035	0.00108
NM_182746.3(MCM4):c.743G>A (p.Arg248His)	rs146842638	0.00029
NM_182746.3(MCM4):c.1929-6T>C	rs567917422	0.00003
NM_182746.3(MCM4):c.2082G>C (p.Ala694=)	rs201709288
NM_182746.3(MCM4):c.2172G>A (p.Arg724=)	rs367938513

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