List of variants in gene ACP5 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_001611.5(ACP5):c.814C>T (p.Arg272Cys)	rs147025508	0.00338
NM_001611.5(ACP5):c.299G>A (p.Arg100His)	rs141651325	0.00096
NM_001611.5(ACP5):c.601C>T (p.Leu201=)	rs568957938	0.00018
NM_001611.5(ACP5):c.702T>C (p.Thr234=)

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