Variant (rsID / SNP)

rs151121191

rs151121191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA2D4. Location: chromosome 12, position 1,965,235. Clinical significance in the table: Likely benign.

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Reference-table entries

CACNA2D4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:1965235
Cytoband: 12p13.33
HGVS: NM_172364.5(CACNA2D4):c.2095C>T (p.Leu699Phe)
Allele change: Missense_L699F

Associated conditions / phenotypes

Retinal cone dystrophy 4

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.