Variant (rsID / SNP)

rs17620

rs17620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF10A. Location: chromosome 8, position 23,060,256. The table records no clinical significance for this variant.

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Reference-table entries

TNFRSF10ANot classified

Variant type: missense_variant
Chromosome / position: 8:23060256
HGVS: NM_003844.4,c.422A>G,p.His141Arg
Allele change: Missense_H141R

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.