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Variant (rsID / SNP)

rs10792447

CDC42BPG

rs10792447 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDC42BPG. Location: chromosome 11, position 64,591,972. The table records no clinical significance for this variant.

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Reference-table entries

CDC42BPGNot classified
Variant type
synonymous_variant
Chromosome / position
11:64591972
HGVS
NM_017525.3,c.4629A>G,p.Leu1543Leu
Allele change
Synonymous_L1543L

Public references

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