Variant (rsID / SNP)

rs687434

rs687434 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GOLGA1. Location: chromosome 9, position 127,643,456. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

GOLGA1Not classified

Variant type: synonymous_variant
Chromosome / position: 9:127643456
HGVS: NM_002077.4,c.2217A>G,p.Glu739Glu
Allele change: Synonymous_E739E

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.