List of variants in gene AGL reported as uncertain significance by Baylor 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000642.3(AGL):c.334A>G (p.Ile112Val)	rs147024351	0.00064
NM_000642.3(AGL):c.4262A>G (p.Asp1421Gly)	rs761264157	0.00009
NM_000642.3(AGL):c.188G>A (p.Arg63His)	rs199958942	0.00006
NM_000642.3(AGL):c.4283A>C (p.Tyr1428Ser)	rs150532164	0.00003
NM_000642.3(AGL):c.3635T>C (p.Met1212Thr)	rs779439947	0.00002
NM_000642.3(AGL):c.1076_1078dup (p.Pro359_His360insPro)	rs750705888
NM_000642.3(AGL):c.1319C>A (p.Ser440Tyr)	rs149771710
NM_000642.3(AGL):c.1735+5G>A
NM_000642.3(AGL):c.2911A>G (p.Ser971Gly)	rs1211367569
NM_000642.3(AGL):c.2930G>T (p.Arg977Leu)	rs147977213
NM_000642.3(AGL):c.3639G>C (p.Gln1213His)	rs1213904866
NM_000642.3(AGL):c.3677T>G (p.Ile1226Arg)	rs749118487

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