List of variants in gene SAMD9L reported as pathogenic for not provided

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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.2957G>A (p.Arg986His)	rs769611275	0.00001
NM_152703.5(SAMD9L):c.1877C>T (p.Ser626Leu)	rs1554341671
NM_152703.5(SAMD9L):c.2640C>A (p.His880Gln)	rs878855336
NM_152703.5(SAMD9L):c.2956C>T (p.Arg986Cys)	rs1554341158
NM_152703.5(SAMD9L):c.4534G>A (p.Val1512Met)	rs2116469012

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