List of variants in gene ALPL reported as 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000478.6(ALPL):c.330T>C (p.Ser110=)	rs1780316	0.92311
NM_000478.6(ALPL):c.876A>G (p.Pro292=)	rs3200255	0.18763
NM_000478.6(ALPL):c.863-46G>A	rs74063110	0.18536
NM_000478.6(ALPL):c.863-12C>G	rs75829132	0.18464
NM_000478.6(ALPL):c.862+20G>T	rs2275377	0.17895
NM_000478.6(ALPL):c.787T>C (p.Tyr263His)	rs3200254	0.17878
NM_000478.6(ALPL):c.863-7T>C	rs74063111	0.17114
NM_000478.6(ALPL):c.793-31C>T	rs1256328	0.13784
NM_000478.6(ALPL):c.1565T>C (p.Val522Ala)	rs34605986	0.07856
NM_000478.6(ALPL):c.1309+46C>T	rs4654760	0.07555
NM_000478.6(ALPL):c.792+45G>T	rs3738098	0.07447
NM_000478.6(ALPL):c.1189+19G>T	rs61778393	0.02227
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.455G>A (p.Arg152His)	rs149344982	0.00814
NM_000478.6(ALPL):c.744C>T (p.Asp248=)	rs188689330	0.00047
NM_000478.6(ALPL):c.1002C>T (p.Gly334=)	rs370122334	0.00026
NM_000478.6(ALPL):c.472+12del	rs35423948

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