Variant (rsID / SNP)

rs2297067

rs2297067 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EXOC3L4. Location: chromosome 14, position 103,566,785. The table records no clinical significance for this variant.

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Reference-table entries

EXOC3L4Not classified

Variant type: missense_variant
Chromosome / position: 14:103566785
HGVS: NM_001077594.2,c.229C>T,p.Arg77Trp
Allele change: Missense_R77W

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.