Variant (rsID / SNP)

rs708775

rs708775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITPKB. Location: chromosome 1, position 226,923,264. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ITPKBNot classified

Variant type: synonymous_variant
Chromosome / position: 1:226923264
HGVS: NM_002221.4,c.1896C>T,p.Ala632Ala
Allele change: Synonymous_A632A

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.