List of variants in gene ALG8 reported as likely benign for digestive system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_024079.5(ALG8):c.175-18C>A	rs73501260	0.00743
NM_024079.5(ALG8):c.175-13A>G	rs186117363	0.00021
NM_024079.5(ALG8):c.154A>G (p.Ile52Val)	rs138293432	0.00019
NM_024079.5(ALG8):c.1178+7A>G	rs766278533	0.00009
NM_024079.5(ALG8):c.1276+10G>A	rs531081999	0.00001
NM_024079.5(ALG8):c.1578A>G (p.Gln526=)	rs479612	0.00001
NM_024079.5(ALG8):c.546+12T>G	rs1169043575	0.00001
NM_024079.5(ALG8):c.1443C>G (p.Thr481=)	rs746756065

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