Variant (rsID / SNP)

rs35344714

rs35344714 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN7A. Location: chromosome 2, position 167,262,169. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SCN7ANot classified

Variant type: missense_variant
Chromosome / position: 2:167262169
HGVS: NM_002976.4,c.4970A>G,p.Asp1657Gly
Allele change: Silent

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.