Variant (rsID / SNP)

rs145846362

rs145846362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF1B. Location: chromosome 1, position 10,384,882. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KIF1BLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:10384882
Cytoband: 1p36.22
HGVS: NM_001365951.3(KIF1B):c.2604C>T (p.Asp868=)
Allele change: Synonymous_D822D

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 2|Neuroblastoma|Charcot-Marie-Tooth 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.