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Variant (rsID / SNP)

rs535586

EHMT2

rs535586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EHMT2. Location: chromosome 6, position 31,860,337. The table records no clinical significance for this variant.

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Reference-table entries

EHMT2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
6:31860337
HGVS
NM_001363689.2,c.882A>G,p.Ser294Ser
Allele change
Synonymous_S237S

Associated conditions / phenotypes

Colorectal Cancer

Public references

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