Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs61747381

ALPK1

rs61747381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK1. Location: chromosome 4, position 113,351,822. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

ALPK1Not classified
Variant type
synonymous_variant
Chromosome / position
4:113351822
HGVS
NM_001102406.2,c.1119G>A,p.Gly373Gly
Allele change
Synonymous_G295G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.