List of variants in gene SPG11 reported as benign by Illumina Laboratory Services, Illumina

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.1388T>C (p.Phe463Ser)	rs3759871	0.48431
NM_025137.4(SPG11):c.3420G>A (p.Leu1140=)	rs36014111	0.03348
NM_025137.4(SPG11):c.2083G>A (p.Ala695Thr)	rs78183930	0.01302
NM_025137.4(SPG11):c.1348A>G (p.Ile450Val)	rs3759873	0.01282
NM_025137.4(SPG11):c.6330G>A (p.Gly2110=)	rs35932349	0.01279
NM_025137.4(SPG11):c.1347C>T (p.Thr449=)	rs3759874	0.01269
NM_025137.4(SPG11):c.3037A>G (p.Lys1013Glu)	rs111347025	0.00958
NM_025137.4(SPG11):c.6319G>A (p.Val2107Ile)	rs115970214	0.00950
NM_025137.4(SPG11):c.3818A>G (p.Lys1273Arg)	rs76389165	0.00694
NM_025137.4(SPG11):c.993C>T (p.Ser331=)	rs76823973	0.00519
NM_025137.4(SPG11):c.1187A>G (p.Tyr396Cys)	rs3759875	0.00006
NM_025137.4(SPG11):c.833A>G (p.Asn278Ser)	rs75309308

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