List of variants in gene ALPL reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.182-15C>G	rs201873253	0.00109
NM_000478.6(ALPL):c.612C>T (p.Ile204=)	rs141448778	0.00067
NM_000478.6(ALPL):c.468C>T (p.Asp156=)	rs143621566	0.00052
NM_000478.6(ALPL):c.863-15T>C	rs373980626	0.00003
NM_000478.6(ALPL):c.1470C>T (p.Ile490=)	rs771120248	0.00002
NM_000478.6(ALPL):c.1190-15C>A	rs1644739262
NM_000478.6(ALPL):c.534C>T (p.Tyr178=)	rs201250289

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