Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs149079952

RHO

rs149079952 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHO. Location: chromosome 3, position 129,247,728. Clinical significance in the table: Benign/Likely benign.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

RHOBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
3:129247728
Cytoband
3q22.1
HGVS
NM_000539.3(RHO):c.152G>C (p.Gly51Ala)
Allele change
Missense_G51A

Associated conditions / phenotypes

Retinitis pigmentosa|Congenital stationary night blindness autosomal dominant 1

Public references

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