List of variants in gene ALPL reported as uncertain significance by Eurofins NTD LLC (GA)

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.818C>T (p.Thr273Met)	rs148405563	0.00106
NM_000478.6(ALPL):c.612C>T (p.Ile204=)	rs141448778	0.00067
NM_000478.6(ALPL):c.1002C>T (p.Gly334=)	rs370122334	0.00026
NM_000478.6(ALPL):c.436G>A (p.Glu146Lys)	rs138587317	0.00015
NM_000478.6(ALPL):c.734C>T (p.Thr245Met)	rs142608957	0.00009
NM_000478.6(ALPL):c.398C>G (p.Ala133Gly)	rs184095519	0.00004
NM_000478.6(ALPL):c.1479C>T (p.Asn493=)	rs759758484	0.00003
NM_000478.6(ALPL):c.673T>C (p.Tyr225His)	rs759125473	0.00003
NM_000478.6(ALPL):c.920C>T (p.Pro307Leu)	rs768555495	0.00001
NM_000478.6(ALPL):c.1004G>C (p.Arg335Thr)	rs1057524727
NM_000478.6(ALPL):c.188G>T (p.Gly63Val)	rs1490668038
NM_000478.6(ALPL):c.921G>A (p.Pro307=)	rs1553414111

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