Variant (rsID / SNP)

rs1003878

rs1003878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSBP1. Location: chromosome 6, position 32,299,822. The table records no clinical significance for this variant.

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Reference-table entries

TSBP1Not classified

Variant type: missense_variant
Chromosome / position: 6:32299822
HGVS: NM_006781.5,c.482C>T,p.Pro161Leu
Allele change: Silent

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.