CASC16

cancer susceptibility 16

Known Variants20 total

rsidPosition (GRCh37)AllelesClassClinVar
rs380366216:52,586,341A/Gcoding sequence variant
rs478422716:52,599,188C/A
rs310474616:52,601,100T/Aintron variant
rs311256216:52,608,263C/Gintron variant
rs6695482816:52,621,220G/Aintron variant
rs310476716:52,624,738G/A
rs311262616:52,625,200A/Gintron variant
rs311262516:52,625,552A/C
rs310476916:52,627,231C/Tintron variant
rs311262116:52,630,349A/T
rs310477616:52,631,462A/T
rs4554423116:52,632,730G/Cintron variant
rs310477816:52,633,652A/Gintron variant
rs1292206116:52,635,000C/Tintron variant
rs311261216:52,635,164G/Aintron variant
rs310478316:52,636,242C/Aintron variant
rs310478816:52,638,503T/A
rs423874916:52,639,234C/Adownstream gene variant
rs111213516:52,639,755C/Tdownstream gene variant
rs310479316:52,641,186T/A

Gene information from NCBI Gene. Variant classifications from ClinVar.