List of variants in gene FAS 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000043.6(FAS):c.369G>A (p.Gln123=)	rs28362318	0.00529
NM_000043.6(FAS):c.580G>A (p.Glu194Lys)	rs56006128	0.00138
NM_000043.6(FAS):c.33T>A (p.Val11=)	rs113022949	0.00135
NM_000043.6(FAS):c.246C>T (p.Cys82=)	rs777751533	0.00001
NM_000043.6(FAS):c.153C>T (p.Gly51=)

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