Variant (rsID / SNP)

rs2667661

rs2667661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TELO2. Location: chromosome 16, position 1,544,302. The table records no clinical significance for this variant.

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Reference-table entries

TELO2Not classified

Variant type: missense_variant
Chromosome / position: 16:1544302
HGVS: NM_001351846.2,c.20A>G,p.Glu7Gly
Allele change: Missense_E7G

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.