ClinVar Miner

List of variants in gene FAM111A reported as likely pathogenic by ClinVar Staff, National Center for Biotechnology Information (NCBI)

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_001312909.2(FAM111A):c.1579C>A (p.Pro527Thr)	rs587777015
NM_001312909.2(FAM111A):c.1583A>G (p.Asp528Gly)	rs587777013

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