Variant (rsID / SNP)

rs2275007

rs2275007 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OSGEP. Location: chromosome 14, position 20,920,250. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

OSGEPNot classified

Variant type: synonymous_variant
Chromosome / position: 14:20920250
HGVS: NM_017807.4,c.294A>G,p.Gln98Gln
Allele change: Synonymous_Q98Q

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.