Variant (rsID / SNP)

rs704

rs704 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VTN. Location: chromosome 17, position 26,694,861. The table records no clinical significance for this variant.

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Reference-table entries

VTNNot classified

Variant type: missense_variant
Chromosome / position: 17:26694861
HGVS: NM_000638.4,c.1199C>T,p.Thr400Met
Allele change: Missense_T400M

Associated conditions / phenotypes

Macular Degeneration, Age-Related, 1|Lung Cancer

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.