Variant (rsID / SNP)

rs4455261

rs4455261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYBB3. Location: chromosome 22, position 25,603,018. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CRYBB3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:25603018
Cytoband: 22q11.23
HGVS: NM_004076.5(CRYBB3):c.475G>A (p.Val159Ile)
Allele change: Missense_V159I

Associated conditions / phenotypes

Cataract 22 multiple types

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.