ClinVar Miner

Submissions for variant NM_005208.5(CRYBA1):c.626C>G (p.Ser209Trp)

dbSNP: rs2153009764
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics England Pilot Project, Genomics England RCV001542604 SCV001760398 likely pathogenic Cataract 10 multiple types no assertion criteria provided clinical testing

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