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Variant (rsID / SNP)

rs12205837

CCDC170

rs12205837 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC170. Location: chromosome 6, position 151,894,340. The table records no clinical significance for this variant.

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Reference-table entries

CCDC170Not classified
Variant type
missense_variant
Chromosome / position
6:151894340
HGVS
NM_025059.4,c.806C>T,p.Ala269Val
Allele change
Missense_A269V

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.