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Variant (rsID / SNP)

rs36062041

EML2

rs36062041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EML2. Location: chromosome 19, position 46,124,531. The table records no clinical significance for this variant.

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Reference-table entries

EML2Not classified
Variant type
synonymous_variant
Chromosome / position
19:46124531
HGVS
NM_001193268.3,c.1659C>T,p.Tyr553Tyr
Allele change
Synonymous_Y330Y

Associated conditions / phenotypes

Synonymous_Y236Y|Synonymous_Y499Y|Synonymous_Y553Y|Silent|Synonymous_Y352Y

Public references

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