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Variant (rsID / SNP)

rs818009

INO80D

rs818009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INO80D. Location: chromosome 2, position 206,921,451. The table records no clinical significance for this variant.

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Reference-table entries

INO80DNot classified
Variant type
synonymous_variant
Chromosome / position
2:206921451
HGVS
NM_017759.5,c.435C>T,p.Thr145Thr
Allele change
Synonymous_T145T

Public references

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