"PreventionGenetics, part of Exact Sciences"[submitter] AND "FAS"[gene - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155871	NM_000043.6(FAS):c.183G>A (p.Lys61=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign
Select item 1566764	NM_000043.6(FAS):c.197-8T>C	FAS	Single nucleotide variant (intron variant)	FAS-related disorder +1 more	GLikely benign
Select item 1406327	NM_000043.6(FAS):c.334+3A>C	FAS	Single nucleotide variant (intron variant)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GUncertain significance
Select item 210992	NM_000043.6(FAS):c.369G>A (p.Gln123=)	FAS	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 856011	NM_000043.6(FAS):c.488C>T (p.Thr163Ile)	FAS (T163I)	Single nucleotide variant (missense variant +1 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GUncertain significance
Select item 1457614	NM_000043.6(FAS):c.528G>A (p.Trp176Ter)	FAS (W176*)	Single nucleotide variant (nonsense +2 more)	Autoimmune lymphoproliferative syndrome type 1 +1 more	GPathogenic
Select item 134374	NM_000043.6(FAS):c.580G>A (p.Glu194Lys)	FAS (E194K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 254734	NM_000043.6(FAS):c.642T>C (p.Thr214=)	FAS	Single nucleotide variant (synonymous variant +2 more)	not specified +2 more	GBenign
Select item 2632730	NM_000043.6(FAS):c.923A>G (p.Glu308Gly)	FAS (E287G +2 more)	Single nucleotide variant (missense variant +2 more)	FAS-related disorder	GUncertain significance