Variant (rsID / SNP)

rs72717434

rs72717434 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EXOC3. Location: chromosome 5, position 447,779. The table records no clinical significance for this variant.

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Reference-table entries

EXOC3Not classified

Variant type: synonymous_variant
Chromosome / position: 5:447779
HGVS: NM_007277.5,c.276C>A,p.Thr92Thr
Allele change: Synonymous_T92T

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.