List of variants in gene ALPL reported as uncertain significance 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.1505C>T (p.Ser502Leu)	rs550358395	0.00029
NM_000478.6(ALPL):c.914C>T (p.Thr305Met)	rs146908399	0.00012
NM_000478.6(ALPL):c.335_340dup (p.Gly112_Thr113dup)	rs931041761
NM_000478.6(ALPL):c.643A>G (p.Ile215Val)

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