ClinVar Miner

List of variants studied for hereditary angioedema type 3 by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000505.4(F12):c.398-12C>T	rs56285942	0.00495
NM_000505.4(F12):c.1272G>C (p.Thr424=)	rs61737766	0.00486
NC_000005.10:g.177409584C>G	rs41309132	0.00297
NM_000505.4(F12):c.-62C>T	rs187018744	0.00223
NM_000505.4(F12):c.983C>A (p.Thr328Lys)	rs118204456

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