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NBN

From SNPedia

is agene
is mentioned by
Full namenibrin
EntrezGene4683
PheGenI4683
VariationViewer4683
ClinVarNBN
GeneCardsNBN
dbSNP4683
SADR4683
HugeNav4683
wikipediaNBN
googleNBN
gopubmedNBN
EVSNBN
HEFalMpNBN
MyGene2NBN
23andMeNBN
UniProtO60934
EnsemblENSG00000104320
OMIM602667
# SNPs66
 Max MagnitudeChromosome positionSummary
i5012770
rs1061302089,946,194
rs106305489,934,373
rs121908973089,964,428
rs121908974089,958,760
rs13312840089,985,681
rs142301194089,937,024
rs1805794089,978,251
rs200287925089,982,766
rs273538389,935,041
rs34767364089,971,232
rs574673404089,984,524
rs587776650689,971,214
rs587780100089,971,174
rs587781305089,981,389
rs587781718089,982,804
rs587781891089,982,770
rs587781969089,955,538
rs587782130089,953,615
rs587782147089,981,512
rs587782344089,953,538
rs587782545089,947,835
rs587782653089,946,211
rs61754966089,978,293
rs709816089,955,483
rs730881839089,970,442
rs730881840089,982,758
rs730881850089,955,281
rs730881857089,943,320
rs730881864089,943,297
rs756363734089,943,252
rs76266447489,981,483
rs766044684089,953,437
rs767215758089,958,819
rs768378152089,981,513
rs769416089,971,229
rs786201745089,953,366
rs786201965089,943,367
rs786202490089,970,451
rs786202494089,981,484
rs786203180089,953,605
rs786203223089,946,138
rs786203662089,971,290
rs786203920089,946,154
rs786204181089,943,272
rs786205135089,970,418
rs86430966889,970,422
rs86430966989,970,417
rs86430967089,970,517
rs864622090089,964,509
... further results


NBN codes for nibrin, a protein with several vital roles within cells, such as DNA repair.

A variant, 657del5 at i5012770, is associated with Nijmegen breakage syndrome. 23andMe reports on this condition.