Variant (rsID / SNP)

rs17325719

rs17325719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCKAP5. Location: chromosome 2, position 133,542,585. The table records no clinical significance for this variant.

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Reference-table entries

NCKAP5Not classified

Variant type: missense_variant
Chromosome / position: 2:133542585
HGVS: NM_207363.3,c.1799G>C,p.Ser600Thr
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.