Variant (rsID / SNP)

rs13280444

rs13280444 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM135B. Location: chromosome 8, position 139,165,273. The table records no clinical significance for this variant.

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Reference-table entries

FAM135BNot classified

Variant type: missense_variant
Chromosome / position: 8:139165273
HGVS: NM_001362965.2,c.1445C>T,p.Pro482Leu
Allele change: Missense_P482L

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.