List of variants in gene ALPL reported as benign by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.876A>G (p.Pro292=)	rs3200255	0.18763
NM_000478.6(ALPL):c.330= (p.Ser110=)	rs1780316	0.07689
NM_000478.6(ALPL):c.1542G>T (p.Ala514=)	rs3200256	0.01113
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.455G>A (p.Arg152His)	rs149344982	0.00814
NM_000478.6(ALPL):c.818C>T (p.Thr273Met)	rs148405563	0.00106
NM_000478.6(ALPL):c.744C>T (p.Asp248=)	rs188689330	0.00047
NM_000478.6(ALPL):c.858A>G (p.Leu286=)	rs375027534	0.00006

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