Variant (rsID / SNP)

rs941591

rs941591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINA10. Location: chromosome 14, position 94,756,750. The table records no clinical significance for this variant.

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Reference-table entries

SERPINA10Not classified

Variant type: missense_variant
Chromosome / position: 14:94756750
HGVS: NM_001100607.3,c.181A>G,p.Ser61Gly
Allele change: Missense_S61G

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.