Variant (rsID / SNP)

rs9982755

rs9982755 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRTAP7-1. Location: chromosome 21, position 32,201,866. The table records no clinical significance for this variant.

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Reference-table entries

KRTAP7-1Not classified

Variant type: missense_variant
Chromosome / position: 21:32201866
HGVS: NM_181606.3,c.151T>C,p.Ser51Pro
Allele change: Missense_S51P

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.