CCDC190

coiled-coil domain containing 190

Known Variants24 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5523352091:162,820,552C/T
rs19124531:162,821,291A/Gdownstream gene variant
rs7633913191:162,824,574G/Tuncertain significance
rs25252250841:162,824,593A/Guncertain significance
rs11883342001:162,824,616G/Alikely benign
rs12592184451:162,824,620A/Cuncertain significance
rs1926517261:162,824,670G/Cuncertain significance
rs7600002551:162,824,686G/Cuncertain significance
rs25252259331:162,824,806C/Tuncertain significance
rs7688629331:162,824,899T/Cuncertain significance
rs1507836721:162,824,952G/Auncertain significance
rs7557436231:162,824,956C/Auncertain significance
rs13098129461:162,825,000G/Auncertain significance
rs16502606591:162,825,062C/Tuncertain significance
rs13674206081:162,825,118A/Tuncertain significance
rs7646904271:162,825,142C/Tuncertain significance
rs25252291051:162,825,486C/Tuncertain significance
rs7506224691:162,825,527A/Guncertain significance
rs16504247981:162,829,321C/Guncertain significance
rs25252383251:162,829,342A/Guncertain significance
rs7560791401:162,829,349G/Anot provided
rs7568477471:162,829,367C/Tuncertain significance
rs15710450961:162,829,403T/Cuncertain significance
rs7704348611:162,829,420A/Guncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.