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Variant (rsID / SNP)

rs3741189

KDM2A

rs3741189 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDM2A. Location: chromosome 11, position 66,995,603. The table records no clinical significance for this variant.

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Reference-table entries

KDM2ANot classified
Variant type
synonymous_variant
Chromosome / position
11:66995603
HGVS
NM_012308.3,c.1053T>C,p.Thr351Thr
Allele change
Synonymous_T351T

Public references

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