ClinVar Miner

List of variants in gene AGPAT2 reported as uncertain significance by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006412.4(AGPAT2):c.809C>T (p.Ala270Val)	rs142417583	0.00634
NM_006412.4(AGPAT2):c.640A>G (p.Lys214Glu)	rs142248792	0.00085

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