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Variant (rsID / SNP)

rs2235258

JARID2

rs2235258 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JARID2. Location: chromosome 6, position 15,513,482. The table records no clinical significance for this variant.

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Reference-table entries

JARID2Not classified
Variant type
synonymous_variant
Chromosome / position
6:15513482
HGVS
NM_004973.4,c.3279G>A,p.Leu1093Leu
Allele change
Synonymous_L1093L

Associated conditions / phenotypes

Schizophrenia

Public references

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