List of variants in gene LRP2 reported as 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_004525.3(LRP2):c.12151+4T>C	rs17848192	0.02665
NM_004525.3(LRP2):c.3452C>T (p.Pro1151Leu)	rs150552608	0.01319
NM_004525.3(LRP2):c.7253A>G (p.Glu2418Gly)	rs61995915	0.01278
NM_004525.3(LRP2):c.13134C>G (p.Pro4378=)	rs73970129	0.01063
NM_004525.3(LRP2):c.13545G>A (p.Gly4515=)	rs34029982	0.00725
NM_004525.3(LRP2):c.79+7G>A	rs376136995	0.00460
NM_004525.3(LRP2):c.9147C>T (p.Phe3049=)	rs146115458	0.00154
NM_004525.3(LRP2):c.9033-9A>G	rs143892351	0.00119
NM_004525.3(LRP2):c.5395-12C>G	rs141206999	0.00108
NM_004525.3(LRP2):c.2511C>T (p.Ala837=)	rs375313914	0.00034
NM_004525.3(LRP2):c.11498-13del	rs143342962
NM_004525.3(LRP2):c.13519-40CT[12]	rs138614485
NM_004525.3(LRP2):c.13519-40CT[13]	rs138614485
NM_004525.3(LRP2):c.428-11_428-8del	rs370823033
NM_004525.3(LRP2):c.428-9_428-8del	rs370823033

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