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Variant (rsID / SNP)

rs11102001

EPS8L3

rs11102001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EPS8L3. Location: chromosome 1, position 110,299,691. The table records no clinical significance for this variant.

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Reference-table entries

EPS8L3Not classified
Variant type
missense_variant
Chromosome / position
1:110299691
HGVS
NM_139053.3,c.1069C>T,p.Pro357Ser
Allele change
Missense_P323S

Public references

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