Variant (rsID / SNP)

rs2273912

rs2273912 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IPO4, REC8. Location: chromosome 14, position 24,649,669. The table records no clinical significance for this variant.

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Reference-table entries

IPO4Not classified

Variant type: synonymous_variant
Chromosome / position: 14:24649669
HGVS: NM_024658.4,c.3225G>A,p.Gln1075Gln
Allele change: Synonymous_Q1075Q

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.