ClinVar Miner

List of variants reported as uncertain significance for MGAT2-congenital disorder of glycosylation by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

Included ClinVar conditions (1):

MGAT2-congenital disorder of glycosylation

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002408.4(MGAT2):c.511C>A (p.Pro171Thr)	rs1327830771
NM_002408.4(MGAT2):c.797C>T (p.Pro266Leu)	rs1566505007

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