Variant (rsID / SNP)

rs6809649

rs6809649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VILL. Location: chromosome 3, position 38,038,982. The table records no clinical significance for this variant.

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Reference-table entries

VILLNot classified

Variant type: synonymous_variant
Chromosome / position: 3:38038982
HGVS: NM_001385038.1,c.570T>C,p.Ala190Ala
Allele change: Synonymous_A190A

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.