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Variant (rsID / SNP)

rs10511

HJURP

rs10511 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HJURP. Location: chromosome 2, position 234,749,258. The table records no clinical significance for this variant.

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Reference-table entries

HJURPNot classified
Variant type
missense_variant
Chromosome / position
2:234749258
HGVS
NM_018410.5,c.2168A>G,p.Glu723Gly
Allele change
Missense_E638G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.