List of variants in gene ALPL reported as likely benign for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.330= (p.Ser110=)	rs1780316	0.07448
NM_000478.6(ALPL):c.455G>A (p.Arg152His)	rs149344982	0.00814
NM_000478.6(ALPL):c.818C>T (p.Thr273Met)	rs148405563	0.00101
NM_000478.6(ALPL):c.612C>T (p.Ile204=)	rs141448778	0.00067
NM_000478.6(ALPL):c.468C>T (p.Asp156=)	rs143621566	0.00050
NM_000478.6(ALPL):c.744C>T (p.Asp248=)	rs188689330	0.00050
NM_000478.6(ALPL):c.649-11G>C	rs376565308	0.00005
NM_000478.6(ALPL):c.1470C>T (p.Ile490=)	rs771120248	0.00002
NM_000478.6(ALPL):c.182-18C>T	rs1644477875
NM_000478.6(ALPL):c.182-5_182-3dup	rs1553411889
NM_000478.6(ALPL):c.62-12C>G
NM_000478.6(ALPL):c.863-15T>A	rs373980626

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