Variant (rsID / SNP)

rs11847654

rs11847654 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EDDM3A. Location: chromosome 14, position 21,215,997. The table records no clinical significance for this variant.

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Reference-table entries

EDDM3ANot classified

Variant type: synonymous_variant
Chromosome / position: 14:21215997
HGVS: NM_006683.5,c.258C>T,p.Ser86Ser
Allele change: Synonymous_S86S

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.