Variant (rsID / SNP)

rs59208852

rs59208852 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR179. Location: chromosome 17, position 36,490,966. Clinical significance in the table: Benign.

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Reference-table entries

GPR179Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:36490966
Cytoband: 17q12
HGVS: NM_001004334.4(GPR179):c.1595G>A (p.Arg532His)
Allele change: Missense_R532H

Associated conditions / phenotypes

Congenital stationary night blindness 1E

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.