List of variants in gene combination ALG1, EEF2KMT reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_019109.5(ALG1):c.1324C>T (p.Arg442Trp)	rs764363207	0.00002
NM_019109.5(ALG1):c.1387G>T (p.Asp463Tyr)	rs765599429	0.00002
NM_019109.5(ALG1):c.1393T>C (p.Ter465Gln)	rs3204229	0.00002
NM_019109.5(ALG1):c.1293G>A (p.Ala431=)	rs1047714	0.00001
NM_019109.5(ALG1):c.1325G>A (p.Arg442Gln)	rs758197753

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