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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
# SNPs101
 Max MagnitudeChromosome positionSummary
i5012770
rs1057516320089,981,430
rs1057516321089,982,721
rs1057516332089,953,501
rs1057516392089,981,516
rs1057516611089,947,890
rs1057516668089,946,236
rs1057516772089,982,719
rs1057516787089,978,273
rs1057516852089,946,209
rs1057516869089,946,160
rs1057517075089,946,138
rs1057517102089,955,556
rs1057517104089,971,172
rs1057517209089,958,724
rs1057517262089,937,076
rs1057519585089,980,884
rs1057519586089,971,194
rs1057519587089,964,480
rs1057519588089,955,555
rs1060503463089,980,831
rs1060503466089,947,881
rs1060503467089,955,282
rs1060503480089,953,536
rs1060503481089,953,438
rs1060503485089,984,536
rs1061302089,946,194
rs1063054089,934,373
rs1064793210089,984,551
rs1064795634089,981,480
rs1064795816089,943,276
rs121908973089,964,428
rs121908974089,958,760
rs13312840089,985,681
rs142301194089,937,024
rs1805794089,978,251
rs200287925089,982,766
rs2735383089,935,041
rs34767364089,971,232
rs574673404089,984,524
rs587776650689,971,214
rs587780096089,980,889
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.