Variant (rsID / SNP)

rs1133618

rs1133618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FKBP15. Location: chromosome 9, position 115,968,797. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FKBP15Not classified

Variant type: missense_variant
Chromosome / position: 9:115968797
HGVS: NM_015258.2,c.316G>A,p.Ala106Thr
Allele change: Missense_A106T

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.