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NBN

From SNPedia

is agene
is mentioned by
Full namenibrin
EntrezGene4683
PheGenI4683
VariationViewer4683
ClinVarNBN
GeneCardsNBN
dbSNP4683
DiseasesNBN
SADR4683
HugeNav4683
wikipediaNBN
googleNBN
gopubmedNBN
EVSNBN
HEFalMpNBN
MyGene2NBN
23andMeNBN
UniProtO60934
EnsemblENSG00000104320
OMIM602667
# SNPs100
 Max MagnitudeChromosome positionSummary
i5012770
rs105751632089,981,430
rs105751632189,982,721
rs105751633289,953,501
rs105751639289,981,516
rs105751661189,947,890
rs105751666889,946,236
rs105751677289,982,719
rs105751678789,978,273
rs105751685289,946,209
rs1057516869
rs105751707589,946,138
rs105751710289,955,556
rs105751710489,971,172
rs105751720989,958,724
rs105751726289,937,076
rs1057519585
rs1057519586
rs1057519587
rs1057519588
rs1060503463
rs1060503466
rs1060503467
rs1060503480
rs1060503481
rs1060503485
rs1061302089,946,194
rs106305489,934,373
rs1064793210
rs1064795634
rs1064795816
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
rs58778009689,980,889
rs587780100089,971,174
rs587781305089,981,389
rs587781718089,982,804
rs587781891089,982,770
rs587781969089,955,538
rs587782130089,953,615
rs587782147089,981,512
rs587782344089,953,538
... 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.