List of variants in gene AGL reported as uncertain significance for not specified

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000642.3(AGL):c.341G>A (p.Arg114His)	rs150146360	0.00011
NM_000642.3(AGL):c.1423+3A>G	rs766117687	0.00008
NM_000642.3(AGL):c.767G>A (p.Arg256His)	rs200180652	0.00004
NM_000642.3(AGL):c.3635T>C (p.Met1212Thr)	rs779439947	0.00002
NM_000642.3(AGL):c.3836+3A>G	rs372921189	0.00002
NM_000642.3(AGL):c.413G>A (p.Gly138Glu)	rs773384152	0.00001
GRCh37/hg19 1p21.2(chr1:100345603-100352899)
NM_000642.3(AGL):c.1027C>T (p.Arg343Trp)	rs1131691438
NM_000642.3(AGL):c.3195T>A (p.Asp1065Glu)	rs569268763
NM_000642.3(AGL):c.4250T>C (p.Leu1417Ser)
NM_000642.3(AGL):c.4514del (p.Asn1505fs)	rs2100901643

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