Variant (rsID / SNP)

rs3731762

rs3731762 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN3A. Location: chromosome 2, position 165,947,256. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SCN3ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:165947256
Cytoband: 2q24.3
HGVS: NM_006922.4(SCN3A):c.5407G>A (p.Asp1803Asn)
Allele change: Missense_D1754N

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.