Variant (rsID / SNP)

rs55752937

rs55752937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK3. Location: chromosome 15, position 85,401,597. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ALPK3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:85401597
Cytoband: 15q25.3
HGVS: NM_020778.5(ALPK3):c.3628C>T (p.Arg1210Trp)
Allele change: Missense_R1412W

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.