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Variant (rsID / SNP)

rs34430497

CCDC170

rs34430497 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC170. Location: chromosome 6, position 151,917,660. The table records no clinical significance for this variant.

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Reference-table entries

CCDC170Not classified
Variant type
missense_variant
Chromosome / position
6:151917660
HGVS
NM_025059.4,c.1658G>A,p.Arg553Gln
Allele change
Missense_R553Q

Public references

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