Variant (rsID / SNP)

rs3209183

rs3209183 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM209B, FAM209A. Location: chromosome 20, position 55,108,617. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FAM209BNot classified

Variant type: missense_variant
Chromosome / position: 20:55108617
HGVS: NM_001013646.4,c.220C>A,p.Gln74Lys
Allele change: Missense_Q74K

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.