Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs6693255

EFCAB7

rs6693255 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFCAB7. Location: chromosome 1, position 63,999,826. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

EFCAB7Not classified
Variant type
missense_variant
Chromosome / position
1:63999826
HGVS
NM_032437.4,c.743C>T,p.Thr248Ile
Allele change
Missense_T248I

Public references

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