Variant (rsID / SNP)

rs1810807

rs1810807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM215. Location: chromosome 9, position 32,784,838. The table records no clinical significance for this variant.

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Reference-table entries

TMEM215Not classified

Variant type: synonymous_variant
Chromosome / position: 9:32784838
HGVS: NM_212558.3,c.657T>C,p.Cys219Cys
Allele change: Synonymous_C219C

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.