List of variants in gene combination SPECC1L, SPECC1L-ADORA2A reported as pathogenic by GeneDx

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_015330.6(SPECC1L):c.1207A>G (p.Met403Val)
NM_015330.6(SPECC1L):c.1244A>G (p.Gln415Arg)	rs387907108
NM_015330.6(SPECC1L):c.1246G>A (p.Ala416Thr)	rs1569420568

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