Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs10749138

NRAP

rs10749138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRAP. Location: chromosome 10, position 115,370,274. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

NRAPNot classified
Variant type
missense_variant
Chromosome / position
10:115370274
HGVS
NM_001261463.2,c.3547A>G,p.Ile1183Val
Allele change
Missense_I1148V

Public references

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