Variant (rsID / SNP)

rs2291260

rs2291260 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GOLGA3. Location: chromosome 12, position 133,357,412. The table records no clinical significance for this variant.

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Reference-table entries

GOLGA3Not classified

Variant type: missense_variant
Chromosome / position: 12:133357412
HGVS: NM_001389683.1,c.3554A>G,p.Lys1185Arg
Allele change: Missense_K1185R

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.