Variant (rsID / SNP)

rs79630438

rs79630438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSN. Location: chromosome 9, position 124,065,219. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

GSNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:124065219
Cytoband: 9q33.2
HGVS: NM_198252.3(GSN):c.227C>T (p.Ala76Val)
Allele change: Missense_A76V

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.