List of variants in gene SLC25A19 reported as uncertain significance for Amish lethal microcephaly

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001126121.2(SLC25A19):c.155G>A (p.Arg52His)	rs138954932	0.00044
NM_001126121.2(SLC25A19):c.622C>T (p.Pro208Ser)	rs200276538	0.00023
NM_001126121.2(SLC25A19):c.504C>T (p.Ser168=)	rs148474667	0.00016
NM_001126121.2(SLC25A19):c.324C>G (p.His108Gln)	rs146573563	0.00010
NM_001126121.2(SLC25A19):c.135T>A (p.Leu45=)	rs373190423	0.00006
NM_001126121.2(SLC25A19):c.93G>A (p.Ala31=)	rs143765189	0.00005
NM_001126121.2(SLC25A19):c.20A>G (p.Lys7Arg)	rs762770947	0.00003
NM_001126121.2(SLC25A19):c.476G>A (p.Arg159His)	rs778166940	0.00001
NM_001126121.2(SLC25A19):c.-170G>A	rs931515557
NM_001126121.2(SLC25A19):c.246C>T (p.His82=)	rs535476833

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