List of variants in gene FAM111A studied for Osteocraniostenosis

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001312909.2(FAM111A):c.1138A>G (p.Ile380Val)	rs755606746	0.00002
NM_001312909.2(FAM111A):c.1579C>A (p.Pro527Thr)	rs587777015
NM_001312909.2(FAM111A):c.1583A>G (p.Asp528Gly)	rs587777013
NM_001312909.2(FAM111A):c.1706G>A (p.Arg569His)	rs587777011
NM_001312909.2(FAM111A):c.1818G>A (p.Met606Ile)	rs1861987262
NM_001312909.2(FAM111A):c.533C>T (p.Ser178Leu)	rs1861767271

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