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Variant (rsID / SNP)

rs6738031

SCN7A

rs6738031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN7A. Location: chromosome 2, position 167,279,922. The table records no clinical significance for this variant.

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Reference-table entries

SCN7ANot classified
Variant type
missense_variant
Chromosome / position
2:167279922
HGVS
NM_002976.4,c.2874G>T,p.Met958Ile
Allele change
Silent

Associated conditions / phenotypes

Hypertension, Essential

Public references

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