List of variants in gene MEGF10 reported as likely benign for not specified

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001256545.2(MEGF10):c.-19+8943A>G	rs79967765	0.00953
NM_001256545.2(MEGF10):c.218+17C>G	rs72786483	0.00257
NM_001256545.2(MEGF10):c.1002C>T (p.His334=)	rs142947482	0.00254
NM_001256545.2(MEGF10):c.3003C>T (p.Ser1001=)	rs35159176	0.00207
NM_001256545.2(MEGF10):c.1626C>T (p.Cys542=)	rs146902993	0.00129
NM_001256545.2(MEGF10):c.3026-8C>T	rs185480820	0.00098
NM_001256545.2(MEGF10):c.1533C>T (p.Asp511=)	rs151266058	0.00046
NM_001256545.2(MEGF10):c.1130+12C>T	rs201836299	0.00032
NM_001256545.2(MEGF10):c.2980+16G>A	rs374003413	0.00017
NM_001256545.2(MEGF10):c.1839G>A (p.Arg613=)	rs199930517	0.00011
NM_001256545.2(MEGF10):c.1130+13T>C	rs746019129	0.00009
NM_001256545.2(MEGF10):c.219-7T>C	rs372782960	0.00009
NM_001256545.2(MEGF10):c.2943G>A (p.Pro981=)	rs371253627	0.00009
NM_001256545.2(MEGF10):c.120C>T (p.Tyr40=)	rs372038844	0.00006
NM_001256545.2(MEGF10):c.522G>A (p.Arg174=)	rs201076330	0.00005
NM_001256545.2(MEGF10):c.-7G>A	rs4620069	0.00003
NM_001256545.2(MEGF10):c.2145G>A (p.Thr715=)	rs200994008	0.00003
NM_001256545.2(MEGF10):c.917+6G>T	rs746095070	0.00002
NM_001256545.2(MEGF10):c.-19+8977C>T	rs559140741	0.00001
NM_001256545.2(MEGF10):c.1008C>T (p.Ser336=)	rs145815113	0.00001
NM_001256545.2(MEGF10):c.116+12G>C	rs775584154	0.00001
NM_001256545.2(MEGF10):c.1278A>G (p.Gly426=)	rs139438683	0.00001
NM_001256545.2(MEGF10):c.2853G>A (p.Thr951=)	rs966689979	0.00001
NM_001256545.2(MEGF10):c.2980+9T>C	rs779077674	0.00001
NM_001256545.2(MEGF10):c.59T>C (p.Ile20Thr)	rs748919606	0.00001
NM_001256545.2(MEGF10):c.930G>A (p.Glu310=)	rs1264341592	0.00001
NM_001256545.2(MEGF10):c.-19+8933A>G	rs1057522065
NM_001256545.2(MEGF10):c.156T>C (p.Phe52=)	rs886038703
NM_001256545.2(MEGF10):c.786A>G (p.Thr262=)	rs893078096

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