Variant (rsID / SNP)

rs2289622

rs2289622 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATG2B. Location: chromosome 14, position 96,771,959. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ATG2BNot classified

Variant type: missense_variant
Chromosome / position: 14:96771959
HGVS: NM_018036.7,c.4700T>C,p.Ile1567Thr
Allele change: Missense_I1567T

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.