ClinVar Miner

List of variants in gene GNAL reported as uncertain significance for Dystonia 25

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_182978.4(GNAL):c.311G>A (p.Gly104Asp)
NM_182978.4(GNAL):c.377-261G>C
NM_182978.4(GNAL):c.764C>T (p.Thr255Ile)	rs1598436429

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