Variant (rsID / SNP)

rs2304240

rs2304240 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ICAM3. Location: chromosome 19, position 10,449,392. The table records no clinical significance for this variant.

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Reference-table entries

ICAM3Not classified

Variant type: synonymous_variant
Chromosome / position: 19:10449392
HGVS: NM_002162.5,c.309T>C,p.Ser103Ser
Allele change: Synonymous_S103S

Associated conditions / phenotypes

Lymphoma, Non-Hodgkin, Familial|Lymphoma, Hodgkin, Classic

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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