List of variants in gene SORL1 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003105.6(SORL1):c.5448T>C (p.Tyr1816=)	rs150315143	0.00262
NM_003105.6(SORL1):c.6318G>A (p.Gln2106=)	rs149393026	0.00104
NM_003105.6(SORL1):c.6021A>G (p.Gln2007=)	rs141089496	0.00065
NM_003105.6(SORL1):c.5023C>T (p.Pro1675Ser)	rs200758028	0.00009
NM_003105.6(SORL1):c.759-5G>T	rs1464131024
NM_003105.6(SORL1):c.759-7C>T	rs751284432

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