Variant (rsID / SNP)

rs6076347

rs6076347 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GINS1. Location: chromosome 20, position 25,398,790. The table records no clinical significance for this variant.

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Reference-table entries

GINS1Not classified

Variant type: missense_variant
Chromosome / position: 20:25398790
HGVS: NM_021067.5,c.289G>A,p.Val97Ile
Allele change: Missense_V97I

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.