Variant (rsID / SNP)

rs34816651

rs34816651 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC171. Location: chromosome 9, position 15,744,683. The table records no clinical significance for this variant.

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Reference-table entries

CCDC171Not classified

Variant type: missense_variant
Chromosome / position: 9:15744683
HGVS: NM_001355547.1,c.2486G>A,p.Cys829Tyr
Allele change: Missense_C821Y

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.