List of variants in gene ASPM reported as pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_018136.5(ASPM):c.9178C>T (p.Gln3060Ter)	rs137852994	0.00015
NM_018136.5(ASPM):c.2419+2T>C	rs587783225	0.00002
NM_018136.5(ASPM):c.3796G>T (p.Glu1266Ter)	rs199422161	0.00001
NM_018136.5(ASPM):c.7160_7161del (p.Ser2387fs)	rs587783265
NM_018136.5(ASPM):c.8195_8196del (p.Arg2732fs)

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