List of variants in gene MIB1 reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_020774.4(MIB1):c.843A>T (p.Thr281=)	rs137957940	0.00231
NM_020774.4(MIB1):c.603T>G (p.Ala201=)	rs35738763	0.00094
NM_020774.4(MIB1):c.2337C>T (p.Leu779=)	rs146430244	0.00037
NM_020774.4(MIB1):c.736T>C (p.Leu246=)	rs188600853	0.00036
NM_020774.4(MIB1):c.2779+8G>A	rs148003129	0.00034
NM_020774.4(MIB1):c.2445C>G (p.Thr815=)	rs150116970	0.00025
NM_020774.4(MIB1):c.1470C>T (p.Val490=)	rs141701856	0.00023
NM_020774.4(MIB1):c.636+7A>C	rs765948951	0.00010
NM_020774.4(MIB1):c.138G>A (p.Glu46=)	rs376396687	0.00004
NM_020774.4(MIB1):c.2325G>A (p.Ser775=)	rs781491471	0.00004
NM_020774.4(MIB1):c.2580G>A (p.Arg860=)	rs762343314	0.00001

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