"Genome-Nilou Lab"[submitter] AND "F13A1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 255186	NM_000129.4(F13A1):c.1954G>C (p.Glu652Gln)	F13A1 (E652Q)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1237919	NM_000129.4(F13A1):c.1909-29G>C	F13A1	Single nucleotide variant (intron variant)	Factor XIII, A subunit, deficiency of +1 more	GBenign
Select item 1237804	NM_000129.4(F13A1):c.1747+27C>G	F13A1	Single nucleotide variant (intron variant)	Factor XIII, A subunit, deficiency of +1 more	GBenign
Select item 255184	NM_000129.4(F13A1):c.1704A>G (p.Glu568=)	F13A1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 255183	NM_000129.4(F13A1):c.1694C>T (p.Pro565Leu)	F13A1 (P565L)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1227355	NM_000129.4(F13A1):c.1217-23C>T	F13A1	Single nucleotide variant (intron variant)	Factor XIII, A subunit, deficiency of +1 more	GBenign
Select item 1253415	NM_000129.4(F13A1):c.1217-24C>T	F13A1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 357680	NM_000129.4(F13A1):c.-19+12A>C	F13A1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar