Variant (rsID / SNP)

rs1395268

rs1395268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINB11. Location: chromosome 18, position 61,377,579. The table records no clinical significance for this variant.

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Reference-table entries

SERPINB11Not classified

Variant type: missense_variant
Chromosome / position: 18:61377579
HGVS: NM_001370475.1,c.152A>C,p.Glu51Ala
Allele change: Missense_E51A

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.