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Variant (rsID / SNP)

rs12801394

CYB5R2PPFIBP2

rs12801394 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYB5R2, PPFIBP2. Location: chromosome 11, position 7,687,715. The table records no clinical significance for this variant.

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Reference-table entries

CYB5R2Not classified
Variant type
missense_variant
Chromosome / position
11:7687715
HGVS
NM_001302826.2,c.625A>G,p.Asn209Asp
Allele change
Missense_N209D

Public references

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