Variant (rsID / SNP)

rs10435864

rs10435864 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FKBP15. Location: chromosome 9, position 115,950,706. The table records no clinical significance for this variant.

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Reference-table entries

FKBP15Not classified

Variant type: missense_variant
Chromosome / position: 9:115950706
HGVS: NM_015258.2,c.1239T>G,p.His413Gln
Allele change: Missense_H413Q

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.