List of variants in gene SLC25A19 reported as likely benign 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)

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001126121.2(SLC25A19):c.483C>T (p.Ala161=)	rs142281464	0.00215
NM_001126121.2(SLC25A19):c.288+8G>C	rs144563813	0.00029
NM_001126121.2(SLC25A19):c.642T>C (p.Asn214=)	rs147091827	0.00021
NM_021734.4(SLC25A19):c.-201T>A	rs576181366

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