LRRC10B

leucine rich repeat containing 10B

Known Variants23 total

rsidPosition (GRCh37)AllelesClassClinVar
rs102636783011:61,276,529G/Auncertain significance
rs254017499211:61,276,549G/Cuncertain significance
rs120503573811:61,276,584C/Guncertain significance
rs147139735511:61,276,594G/Tuncertain significance
rs75888875811:61,276,610A/Guncertain significance
rs76301443111:61,276,698C/Auncertain significance
rs126445647211:61,276,833G/Cuncertain significance
rs254017558211:61,276,905C/Auncertain significance
rs75679977411:61,276,978C/Auncertain significance
rs254017610311:61,277,092G/Cuncertain significance
rs77342619511:61,277,161G/Auncertain significance
rs90376631611:61,277,176C/Auncertain significance
rs91030752211:61,277,218C/Tuncertain significance
rs254017641111:61,277,246A/Guncertain significance
rs254017641411:61,277,248G/Auncertain significance
rs57172645511:61,277,251G/Auncertain significance
rs124709198211:61,277,257G/Auncertain significance
rs53439862611:61,277,323G/Auncertain significance
rs76132717511:61,277,329G/Auncertain significance
rs254017664911:61,277,341G/Auncertain significance
rs1123072811:61,277,698A/Gdownstream gene variant
rs1089716411:61,277,775A/C
rs75198511:61,278,590C/Tdownstream gene variant

Gene information from NCBI Gene. Variant classifications from ClinVar.