Variant (rsID / SNP)

rs4802605

rs4802605 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFY. Location: chromosome 19, position 49,930,721. The table records no clinical significance for this variant.

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Reference-table entries

GFYNot classified

Variant type: missense_variant
Chromosome / position: 19:49930721
HGVS: NM_001195256.2,c.1034T>C,p.Val345Ala
Allele change: Missense_V345A

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.