ClinVar Miner

List of variants reported as benign for cone-rod dystrophy 13 by Molecular Genetics, Royal Melbourne Hospital

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_020366.4(RPGRIP1):c.1639G>T (p.Ala547Ser) rs10151259 0.21790

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