Variant (rsID / SNP)

rs61734295

rs61734295 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM1. Location: chromosome 15, position 31,294,159. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TRPM1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:31294159
Cytoband: 15q13.3
HGVS: NM_001252024.2(TRPM1):c.4744G>A (p.Val1582Met)
Allele change: Missense_V1560M

Associated conditions / phenotypes

Congenital stationary night blindness 1C

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.