Variant (rsID / SNP)

rs61731112

rs61731112 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNR. Location: chromosome 1, position 175,372,714. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TNRConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 1:175372714
Cytoband: 1q25.1
HGVS: NM_003285.3(TNR):c.538A>C (p.Asn180His)
Allele change: Missense_N180H

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.