Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs140687140

TREH

rs140687140 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TREH. Location: chromosome 11, position 118,531,335. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TREHNot classified
Variant type
missense_variant
Chromosome / position
11:118531335
HGVS
NM_007180.3,c.1015A>G,p.Ile339Val
Allele change
Missense_I308V

Public references

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