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Variant (rsID / SNP)

rs7322112

CCDC168

rs7322112 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC168. Location: chromosome 13, position 103,391,634. The table records no clinical significance for this variant.

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Reference-table entries

CCDC168Not classified
Variant type
missense_variant
Chromosome / position
13:103391634
HGVS
NM_001146197.3,c.11413G>A,p.Val3805Ile
Allele change
Missense_V3805I

Public references

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