Variant (rsID / SNP)
rs74871223
rs74871223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR179. Location: chromosome 17, position 36,499,019. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
GPR179Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:36499019
- Cytoband
- 17q12
- HGVS
- NM_001004334.4(GPR179):c.654T>G (p.Asp218Glu)
- Allele change
- Missense_D218E
Associated conditions / phenotypes
Congenital stationary night blindness 1E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.