Variant (rsID / SNP)

rs3823482

rs3823482 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM209. Location: chromosome 7, position 129,813,738. The table records no clinical significance for this variant.

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Reference-table entries

TMEM209Not classified

Variant type: synonymous_variant
Chromosome / position: 7:129813738
HGVS: NM_032842.4,c.1386A>G,p.Leu462Leu
Allele change: Synonymous_L420L

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.