ClinVar for MedGen (Select 482302) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 143996	NM_000506.5(F2):c.1726-59G>A	F2	Single nucleotide variant (intron variant)	Pregnancy loss, recurrent, susceptibility to, 2 +4 more	GBenign
Select item 13310	NM_000506.5(F2):c.*97G>A	F2	Single nucleotide variant	Venous thromboembolism +4 more	GPathogenic/Likely pathogenic/Pathogenic, low penetrance; risk factor