List of variants in gene STAR 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000349.3(STAR):c.361C>T (p.Arg121Trp)	rs34908868	0.00193
NM_000349.3(STAR):c.141G>A (p.Thr47=)	rs147318238	0.00173
NM_000349.3(STAR):c.120G>A (p.Leu40=)	rs138786388

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