List of variants in gene ASPM reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_018136.5(ASPM):c.5821T>C (p.Cys1941Arg)	rs61249253	0.01514
NM_018136.5(ASPM):c.7917A>G (p.Lys2639=)	rs112647911	0.00953
NM_018136.5(ASPM):c.8820+7C>G	rs115045814	0.00865
NM_018136.5(ASPM):c.5185C>T (p.Arg1729Trp)	rs41299623	0.00808
NM_018136.5(ASPM):c.5206C>G (p.Gln1736Glu)	rs62623455	0.00788
NM_018136.5(ASPM):c.7565T>G (p.Leu2522Ter)	rs62624965	0.00780
NM_018136.5(ASPM):c.2218A>T (p.Ile740Leu)	rs35203521	0.00779
NM_018136.5(ASPM):c.644A>C (p.Glu215Ala)	rs114695225	0.00779
NM_018136.5(ASPM):c.1451A>G (p.Asn484Ser)	rs114737609	0.00775
NM_018136.5(ASPM):c.10162-7T>A	rs141402675	0.00774
NM_018136.5(ASPM):c.9773A>G (p.His3258Arg)	rs7528827	0.00754
NM_018136.5(ASPM):c.3741+3A>G	rs138558822	0.00656
NM_018136.5(ASPM):c.6727G>T (p.Val2243Leu)	rs148425392	0.00493
NM_018136.5(ASPM):c.4213C>T (p.Arg1405Cys)	rs139367209	0.00396
NM_018136.5(ASPM):c.3791G>A (p.Arg1264His)	rs150125249	0.00378

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