Variant (rsID / SNP)

rs35156678

rs35156678 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EML3, MTA2. Location: chromosome 11, position 62,369,881. The table records no clinical significance for this variant.

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Reference-table entries

EML3Not classified

Variant type: stop_gained
Chromosome / position: 11:62369881
HGVS: NM_001300793.2,c.2650C>T,p.Gln884*
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.