List of variants in gene SAMD9L reported as likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_152703.5(SAMD9L):c.3102T>C (p.Asp1034=)	rs75823828	0.01398
NM_152703.5(SAMD9L):c.3964T>C (p.Leu1322=)	rs73710962	0.00818
NM_152703.5(SAMD9L):c.2114A>G (p.Tyr705Cys)	rs144236612	0.00009
NM_152703.5(SAMD9L):c.1015C>A (p.Leu339Ile)	rs138238924	0.00007
NM_152703.5(SAMD9L):c.2316T>G (p.Thr772=)	rs201861233	0.00005

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