ClinVar Miner

List of variants in gene GABRB1 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000812.4(GABRB1):c.1108A>G (p.Ser370Gly)	rs767031899	0.00002
NM_000812.4(GABRB1):c.74C>G (p.Ala25Gly)	rs1725307754	0.00001

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