Variant (rsID / SNP)

rs56149652

rs56149652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SELENOV. Location: chromosome 19, position 40,009,396. The table records no clinical significance for this variant.

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Reference-table entries

SELENOVNot classified

Variant type: missense_variant
Chromosome / position: 19:40009396
HGVS: NM_182704.2,c.851A>G,p.Lys284Arg
Allele change: Missense_K284R

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.