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Variant (rsID / SNP)

rs10202624

EML4

rs10202624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EML4. Location: chromosome 2, position 42,515,388. The table records no clinical significance for this variant.

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Reference-table entries

EML4Not classified
Variant type
missense_variant
Chromosome / position
2:42515388
HGVS
NM_019063.5,c.1144A>G,p.Ile382Val
Allele change
Missense_I382V

Public references

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