Variant (rsID / SNP)

rs17592459

rs17592459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC168. Location: chromosome 13, position 103,388,880. The table records no clinical significance for this variant.

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Reference-table entries

CCDC168Not classified

Variant type: missense_variant
Chromosome / position: 13:103388880
HGVS: NM_001146197.3,c.14167A>G,p.Met4723Val
Allele change: Missense_M4723V

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.