Variant (rsID / SNP)

rs929509

rs929509 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLCCI1. Location: chromosome 7, position 8,125,964. The table records no clinical significance for this variant.

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Reference-table entries

GLCCI1Not classified

Variant type: synonymous_variant
Chromosome / position: 7:8125964
HGVS: NM_138426.4,c.1440C>T,p.Ser480Ser
Allele change: Synonymous_S480S

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.