Variant (rsID / SNP)

rs6599528

rs6599528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADCK5. Location: chromosome 8, position 145,603,114. The table records no clinical significance for this variant.

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Reference-table entries

ADCK5Not classified

Variant type: missense_variant
Chromosome / position: 8:145603114
HGVS: NM_174922.5,c.51A>C,p.Arg17Ser
Allele change: Missense_R17S

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.