Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs3847531

FAT3

rs3847531 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT3. Location: chromosome 11, position 92,534,442. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

FAT3Not classified
Variant type
missense_variant
Chromosome / position
11:92534442
HGVS
NM_001367949.2,c.8263A>G,p.Ile2755Val
Allele change
Missense_I2755V

Public references

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