List of variants in gene C19orf12 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_031448.6(C19orf12):c.214C>T (p.Pro72Ser)	rs1487944357	0.00001
NM_031448.6(C19orf12):c.221C>G (p.Pro74Arg)	rs747900430	0.00001
NM_031448.6(C19orf12):c.200G>A (p.Ser67Asn)

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