List of variants in gene C19orf12 reported as not provided for central nervous system disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_031448.6(C19orf12):c.391A>G (p.Lys131Glu)	rs146170087	0.00094
NM_031448.6(C19orf12):c.154G>C (p.Ala52Pro)	rs376103979	0.00013
NM_031448.6(C19orf12):c.-2C>T	rs397514477	0.00003
NM_031448.6(C19orf12):c.171_181del (p.Gly58fs)	rs515726204

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