Variant (rsID / SNP)

rs1891110

rs1891110 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM24B. Location: chromosome 10, position 124,610,027. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FAM24BNot classified

Variant type: missense_variant
Chromosome / position: 10:124610027
HGVS: NM_001204364.1,c.5C>T,p.Pro2Leu
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.