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Variant (rsID / SNP)

rs2275799

NRAP

rs2275799 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRAP. Location: chromosome 10, position 115,409,840. The table records no clinical significance for this variant.

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Reference-table entries

NRAPNot classified
Variant type
missense_variant
Chromosome / position
10:115409840
HGVS
NM_001261463.2,c.844G>A,p.Ala282Thr
Allele change
Missense_A282T

Public references

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