Variant (rsID / SNP)

rs3806589

rs3806589 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HJURP. Location: chromosome 2, position 234,750,831. The table records no clinical significance for this variant.

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Reference-table entries

HJURPNot classified

Variant type: missense_variant
Chromosome / position: 2:234750831
HGVS: NM_018410.5,c.595A>G,p.Arg199Gly
Allele change: Missense_R114G

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.