Variant (rsID / SNP)

rs115379833

rs115379833 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RELN. Location: chromosome 7, position 103,191,588. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RELNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:103191588
Cytoband: 7q22.1
HGVS: NM_005045.4(RELN):c.6228C>T (p.Ser2076=)
Allele change: Synonymous_S2076S

Associated conditions / phenotypes

Norman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7

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.