Variant (rsID / SNP)

rs14326

rs14326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GNG4. Location: chromosome 1, position 235,715,523. The table records no clinical significance for this variant.

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Reference-table entries

GNG4Not classified

Variant type: synonymous_variant
Chromosome / position: 1:235715523
HGVS: NM_001098721.2,c.114T>C,p.Ala38Ala
Allele change: Synonymous_A38A

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.