List of variants in gene SALL1 reported as uncertain significance 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: 5

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HGVS	dbSNP
NM_002968.2(SALL1):c.1405C>T (p.Arg469Cys)	rs1057523061
NM_002968.2(SALL1):c.3157A>C (p.Met1053Leu)	rs1057523060
NM_002968.2(SALL1):c.3601G>A (p.Gly1201Ser)	rs1555474728
NM_002968.2(SALL1):c.3938G>A (p.Arg1313His)	rs529030284
NM_002968.2(SALL1):c.477_478insAGCGGC (p.Gly160_Gly161insSerGly)	rs1555475415

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