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Variant (rsID / SNP)

rs34133636

CCDC150

rs34133636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC150. Location: chromosome 2, position 197,521,750. The table records no clinical significance for this variant.

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Reference-table entries

CCDC150Not classified
Variant type
missense_variant
Chromosome / position
2:197521750
HGVS
NM_001080539.2,c.466G>A,p.Glu156Lys
Allele change
Silent

Public references

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