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Variant (rsID / SNP)

rs4404487

HEG1

rs4404487 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEG1. Location: chromosome 3, position 124,746,347. The table records no clinical significance for this variant.

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Reference-table entries

HEG1Not classified
Variant type
synonymous_variant
Chromosome / position
3:124746347
HGVS
NM_020733.2,c.615A>G,p.Ser205Ser
Allele change
Synonymous_S205S

Public references

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