List of variants in gene ALMS1 reported as likely benign by Pars Genome Lab

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378454.1(ALMS1):c.9822C>G (p.Thr3274=)	rs201446579	0.00245
NM_001378454.1(ALMS1):c.10238A>G (p.Glu3413Gly)	rs184779459	0.00032
NM_001378454.1(ALMS1):c.11748G>A (p.Glu3916=)	rs373364340	0.00007

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