Variant (rsID / SNP)

rs8099409

rs8099409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM241. Location: chromosome 18, position 20,953,720. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TMEM241Not classified

Variant type: missense_variant
Chromosome / position: 18:20953720
HGVS: NM_032933.6,c.391C>T,p.Leu131Phe
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.