Variant (rsID / SNP)

rs909341

rs909341 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF6B. Location: chromosome 20, position 62,328,742. The table records no clinical significance for this variant.

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Reference-table entries

TNFRSF6BNot classified

Variant type: synonymous_variant
Chromosome / position: 20:62328742
HGVS: NM_003823.4,c.486C>T,p.Ser162Ser
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.