List of variants in gene combination ACTA2, FAS reported as likely benign for autoimmune disease

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001141945.3(ACTA2):c.-24+357C>T	rs9658677	0.00433
NM_001141945.3(ACTA2):c.-24+409G>A	rs56220100	0.00346
NM_000043.6(FAS):c.27T>C (p.Pro9=)	rs1847138768
NM_000043.6(FAS):c.30+14_30+18dup	rs2494798072
NM_000043.6(FAS):c.30+19G>T	rs202165529
NM_000043.6(FAS):c.30+20G>A	rs2494798564
NM_000043.6(FAS):c.4C>T (p.Leu2=)	rs774656178
NM_001141945.3(ACTA2):c.-24+414_-24+415del	rs553556054

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