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KDM5B

From SNPedia
is agene
is mentioned by
Full namelysine (K)-specific demethylase 5B
EntrezGene10765
PheGenI10765
VariationViewer10765
ClinVarKDM5B
GeneCardsKDM5B
dbSNP10765
DiseasesKDM5B
SADR10765
HugeNav10765
wikipediaKDM5B
googleKDM5B
gopubmedKDM5B
EVSKDM5B
HEFalMpKDM5B
MyGene2KDM5B
23andMeKDM5B
UniProtQ9UGL1
EnsemblENSG00000117139
OMIM605393
# SNPs1
 Max MagnitudeChromosome positionSummary
rs104948360202,727,750

https://www.genomicseducation.hee.nhs.uk/news/item/167-answers-for-100-000-genomes-project-participants a spontaneous mutation in this gene is the source of http://ghr.nlm.nih.gov/condition/glut1-deficiency-syndrome