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Variant (rsID / SNP)

rs3127122

NRAP

rs3127122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRAP. Location: chromosome 10, position 115,422,474. The table records no clinical significance for this variant.

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Reference-table entries

NRAPNot classified
Variant type
synonymous_variant
Chromosome / position
10:115422474
HGVS
NM_001261463.2,c.219T>C,p.Asn73Asn
Allele change
Synonymous_N73N

Public references

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