Variant (rsID / SNP)

rs33988592

rs33988592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GOLGB1. Location: chromosome 3, position 121,415,610. The table records no clinical significance for this variant.

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Reference-table entries

GOLGB1Not classified

Variant type: missense_variant
Chromosome / position: 3:121415610
HGVS: NM_001256486.2,c.3760C>T,p.Pro1254Ser
Allele change: Missense_P1249S

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.