Variant (rsID / SNP)

rs1539172

rs1539172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC171. Location: chromosome 9, position 15,784,631. The table records no clinical significance for this variant.

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Reference-table entries

CCDC171Not classified

Variant type: missense_variant
Chromosome / position: 9:15784631
HGVS: NM_001355547.1,c.3230A>G,p.Lys1077Arg
Allele change: Missense_K1069R

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.