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Variant (rsID / SNP)

rs72741390

PFKFB2

rs72741390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PFKFB2. Location: chromosome 1, position 207,238,419. The table records no clinical significance for this variant.

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Reference-table entries

PFKFB2Not classified
Variant type
synonymous_variant
Chromosome / position
1:207238419
HGVS
NM_006212.2,c.546C>T,p.Asn182Asn
Allele change
Synonymous_N182N

Public references

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