Variant (rsID / SNP)

rs411254

rs411254 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRTAP10-8, TSPEAR. Location: chromosome 21, position 46,032,094. The table records no clinical significance for this variant.

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Reference-table entries

KRTAP10-8Not classified

Variant type: missense_variant
Chromosome / position: 21:46032094
HGVS: NM_198695.2,c.77A>G,p.His26Arg
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.