Variant (rsID / SNP)

rs150331590

rs150331590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNR. Location: chromosome 1, position 175,375,388. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TNRUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:175375388
Cytoband: 1q25.1
HGVS: NM_003285.3(TNR):c.463T>A (p.Cys155Ser)
Allele change: Missense_C155S

Associated conditions / phenotypes

Parkinson disease

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.