Variant (rsID / SNP)

rs3820246

rs3820246 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF26B. Location: chromosome 1, position 245,849,729. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KIF26BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:245849729
Cytoband: 1q44
HGVS: NM_018012.4(KIF26B):c.3444G>A (p.Pro1148=)
Allele change: Synonymous_P1148P

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.