Variant (rsID / SNP)

rs11210870

rs11210870 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SF3A3. Location: chromosome 1, position 38,449,910. The table records no clinical significance for this variant.

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Reference-table entries

SF3A3Not classified

Variant type: synonymous_variant
Chromosome / position: 1:38449910
HGVS: NM_006802.4,c.399A>G,p.Glu133Glu
Allele change: Synonymous_E80E

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.