ClinVar Miner

List of variants studied for prekallikrein deficiency 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000892.5(KLKB1):c.1072A>G (p.Thr358Ala)	rs4253379	0.01167
NM_000892.5(KLKB1):c.519A>G (p.Gly173=)	rs4253350	0.01158
NM_000892.5(KLKB1):c.808A>G (p.Thr270Ala)	rs113884104	0.00344
NM_000892.5(KLKB1):c.1581G>C (p.Glu527Asp)

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