Variant (rsID / SNP)

rs215561

rs215561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM239. Location: chromosome 20, position 2,797,015. The table records no clinical significance for this variant.

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Reference-table entries

TMEM239Not classified

Variant type: missense_variant
Chromosome / position: 20:2797015
HGVS: NM_001318207.1,c.35G>A,p.Arg12His
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.