ClinVar Miner

List of variants in gene CFC1 reported as benign for heterotaxy, visceral, 2, autosomal

Included ClinVar conditions (1):

Heterotaxy, visceral, 2, autosomal

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032545.4(CFC1):c.484T>C (p.Phe162Leu)	rs776829911	0.00561
NM_032545.4(CFC1):c.433G>A (p.Ala145Thr)	rs199715380

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