ClinVar Miner

List of variants in gene combination GRM6, ZNF454 reported as likely benign for GRM6-related retinopathy

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_000843.4(GRM6):c.1307C>T (p.Thr436Ile) rs5019554 0.00766
NM_000843.4(GRM6):c.1875C>T (p.Tyr625=) rs62638215 0.00277
NM_000843.4(GRM6):c.2054C>G (p.Ser685Trp) rs144657366

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