CEP85L, centrosomal protein 85 like, 387119

N. diseases: 40; N. variants: 12
Disease: QT interval feature (observable entity) ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11756438
rs11756438 		0.925 0.040 6 118672469 intron variant C/A snv 0.42
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 2 2009 2019
dbSNP: rs11752626
rs11752626 		6 118467489 intron variant G/T snv 0.35
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2019 2019
dbSNP: rs3902035
rs3902035 		6 118679069 intron variant T/C snv 0.22
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2014 2014