List of variants in gene ALPL reported as likely benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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_000478.6(ALPL):c.1381G>A (p.Val461Ile)	rs34810399	0.00860
NM_000478.6(ALPL):c.1119C>T (p.Thr373=)	rs112335417	0.00852
NM_000478.6(ALPL):c.859T>C (p.Leu287=)	rs141742288	0.00141
NM_000478.6(ALPL):c.1505C>T (p.Ser502Leu)	rs550358395	0.00029
NM_000478.6(ALPL):c.858A>G (p.Leu286=)	rs375027534	0.00006

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