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Variant (rsID / SNP)

rs849526

NRP2

rs849526 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRP2. Location: chromosome 2, position 206,592,695. The table records no clinical significance for this variant.

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Reference-table entries

NRP2Not classified
Variant type
synonymous_variant
Chromosome / position
2:206592695
HGVS
NM_201266.2,c.1071T>C,p.Tyr357Tyr
Allele change
Synonymous_Y357Y

Associated conditions / phenotypes

Synonymous_Y357Y

Public references

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