Variant (rsID / SNP)

rs200861589

rs200861589 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINB6. Location: chromosome 6, position 2,954,832. Clinical significance in the table: Likely benign.

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Reference-table entries

SERPINB6Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:2954832
Cytoband: 6p25.2
HGVS: NM_004568.6(SERPINB6):c.424A>G (p.Thr142Ala)
Allele change: Missense_T161A

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.