Variant (rsID / SNP)

rs2270893

rs2270893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMCC3. Location: chromosome 12, position 94,972,290. The table records no clinical significance for this variant.

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Reference-table entries

TMCC3Not classified

Variant type: synonymous_variant
Chromosome / position: 12:94972290
HGVS: NM_020698.4,c.1011G>A,p.Glu337Glu
Allele change: Synonymous_E337E

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.