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Variant (rsID / SNP)

rs2289233

ITM2C

rs2289233 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITM2C. Location: chromosome 2, position 231,738,269. The table records no clinical significance for this variant.

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Reference-table entries

ITM2CNot classified
Variant type
synonymous_variant
Chromosome / position
2:231738269
HGVS
NM_001287241.2,c.258G>A,p.Ala86Ala
Allele change
Synonymous_A86A

Public references

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