List of variants reported as likely benign for metachromatic leukodystrophy due to saposin B deficiency by Illumina Laboratory Services, Illumina

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002778.4(PSAP):c.204C>T (p.Asp68=)	rs143981174	0.00484
NM_002778.4(PSAP):c.1380C>T (p.Pro460=)	rs1049882	0.00284
NM_002778.4(PSAP):c.88G>T (p.Ala30Ser)	rs144942998	0.00051
NM_002778.4(PSAP):c.-29C>T	rs201780377	0.00035
NM_002778.4(PSAP):c.336C>T (p.Ser112=)	rs370977178	0.00003

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