ClinVar Miner

List of variants in gene FIBP, LOC130006079 studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004214.5(FIBP):c.712A>C (p.Lys238Gln)	rs2134771616
NM_004214.5(FIBP):c.721G>C (p.Val241Leu)
NM_004214.5(FIBP):c.724G>T (p.Ala242Ser)

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