Variant (rsID / SNP)

rs2715687

rs2715687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GUCA1C. Location: chromosome 3, position 108,639,423. The table records no clinical significance for this variant.

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Reference-table entries

GUCA1CNot classified

Variant type: missense_variant
Chromosome / position: 3:108639423
HGVS: NM_005459.4,c.214G>A,p.Val72Ile
Allele change: Missense_V72I

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.