List of variants in gene ASPM reported as benign by Eurofins NTD LLC (GA)

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_018136.5(ASPM):c.7480T>C (p.Tyr2494His)	rs964201	0.99668
NM_018136.5(ASPM):c.7566A>G (p.Leu2522=)	rs1412640	0.80210
NM_018136.5(ASPM):c.10331+8A>G	rs10754213	0.77181
NM_018136.5(ASPM):c.441+14C>T	rs1571964	0.74895
NM_018136.5(ASPM):c.849C>T (p.Ser283=)	rs6677082	0.74886
NM_018136.5(ASPM):c.4449A>G (p.Lys1483=)	rs2878749	0.30404
NM_018136.5(ASPM):c.2174-20T>C	rs4915344	0.16253
NM_018136.5(ASPM):c.3269C>T (p.Ser1090Phe)	rs16841081	0.04499
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.3742-10T>G	rs41299587	0.00665
NM_018136.5(ASPM):c.3741+3A>G	rs138558822	0.00656
NM_018136.5(ASPM):c.4213C>T (p.Arg1405Cys)	rs139367209	0.00396
NM_018136.5(ASPM):c.7554A>G (p.Arg2518=)	rs140248383	0.00393
NM_018136.5(ASPM):c.6775T>C (p.Leu2259=)	rs140922974	0.00333
NM_018136.5(ASPM):c.9444+8T>G	rs140150599	0.00278
NM_018136.5(ASPM):c.9996T>C (p.Thr3332=)	rs139927527	0.00253
NM_018136.5(ASPM):c.1385A>G (p.Tyr462Cys)	rs143294539	0.00155
NM_018136.5(ASPM):c.1007C>A (p.Thr336Lys)	rs112113370	0.00066
NM_018136.5(ASPM):c.844A>C (p.Asn282His)	rs113777932	0.00066
NM_018136.5(ASPM):c.905G>A (p.Cys302Tyr)	rs77736715	0.00066
NM_018136.5(ASPM):c.8166T>C (p.Tyr2722=)	rs78315399	0.00046
NM_018136.5(ASPM):c.581C>A (p.Ala194Asp)	rs141532484	0.00038
NM_018136.5(ASPM):c.7475G>A (p.Arg2492Lys)	rs118010078	0.00037
NM_018136.5(ASPM):c.5224T>C (p.Tyr1742His)	rs143733126	0.00019
NM_018136.5(ASPM):c.9539A>C (p.Gln3180Pro)	rs193251130	0.00009
NM_018136.5(ASPM):c.2914T>G (p.Leu972Val)	rs552158003	0.00006

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