List of variants in gene SAMD9L reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152703.5(SAMD9L):c.2640C>A (p.His880Gln)	rs878855336
NM_152703.5(SAMD9L):c.2658_2659del (p.Phe886fs)	rs2116486108
NM_152703.5(SAMD9L):c.3587G>C (p.Cys1196Ser)	rs878855337

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