Variant (rsID / SNP)

rs61743088

rs61743088 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROS1. Location: chromosome 6, position 117,715,395. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ROS1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 6:117715395
Cytoband: 6q22.1
HGVS: NM_001378902.1(ROS1):c.1121G>C (p.Gly374Ala)
Allele change: Missense_G365A

Associated conditions / phenotypes

Abnormality of brain morphology

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.