Variant (rsID / SNP)

rs7318267

rs7318267 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FARP1. Location: chromosome 13, position 98,896,776. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FARP1Not classified

Variant type: missense_variant
Chromosome / position: 13:98896776
HGVS: NM_001001715.4,c.203C>T,p.Thr68Ile
Allele change: Silent

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.