List of variants in gene ALG9 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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_024740.2(ALG9):c.*2473A>T	rs2554994	0.69652
NM_024740.2(ALG9):c.*2474A>T	rs376483443	0.04275
NM_024740.2(ALG9):c.*1607C>T	rs117488631	0.00826
NM_024740.2(ALG9):c.*1624A>C	rs117091304	0.00485
NM_024740.2(ALG9):c.*1722C>T	rs186477879	0.00192
NM_024740.2(ALG9):c.*314G>A	rs781928817	0.00077
NM_024740.2(ALG9):c.*523T>C	rs536072357	0.00006
NM_024740.2(ALG9):c.*1679del	rs150703313
NM_024740.2(ALG9):c.2473_2474insT	rs886047666
NM_024740.2(ALG9):c.*2479del	rs376955296

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