Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs10770136

IRAG1

rs10770136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRAG1. Location: chromosome 11, position 10,715,124. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

IRAG1Not classified
Variant type
missense_variant
Chromosome / position
11:10715124
HGVS
NM_130385.4,c.26A>G,p.Glu9Gly
Allele change
Silent

Public references

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