LINC01122

long intergenic non-protein coding RNA 1122

Known Variants38 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs764975	2:58,761,599	A/G	intron variant	—
rs7608397	2:58,769,042	G/T	intron variant	—
rs72813970	2:58,787,801	G/A	intron variant	—
rs6736025	2:58,797,634	G/T	intron variant	—
rs6718563	2:58,805,945	A/C	intron variant	—
rs6731302	2:58,833,493	A/T	—	—
rs6545695	2:58,849,989	G/A	intron variant	—
rs10190169	2:58,854,942	C/T	—	—
rs1922786	2:58,863,573	A/T	—	—
rs116168752	2:58,864,684	T/C	intron variant	—
rs6724384	2:58,879,493	C/T	intron variant	—
rs74515651	2:58,883,109	C/T	intron variant	—
rs58857776	2:58,890,684	C/A	—	—
rs1861413	2:58,892,962	A/G	regulatory region variant	—
rs1861412	2:58,893,065	G/A	regulatory region variant	—
rs60635548	2:58,916,786	A/G	intron variant	—
rs4541244	2:58,917,535	C/A	—	—
rs13417036	2:58,921,777	G/T	—	—
rs2708146	2:58,955,953	A/G	intron variant	—
rs13428870	2:58,956,557	T/G	intron variant	—
rs12619538	2:58,963,236	A/C	intron variant	—
rs1641154	2:58,969,997	G/C	intron variant	—
rs2540323	2:58,973,397	T/A	intron variant	—
rs7596101	2:58,978,436	A/C	—	—
rs77732866	2:58,979,879	G/A	intron variant	—
rs727857	2:58,981,967	G/A	intron variant	—
rs12613375	2:58,984,109	C/T	intron variant	—
rs10865309	2:58,984,870	C/T	intron variant	—
rs76341179	2:58,985,375	C/T	intron variant	—
rs62144565	2:59,034,951	G/T	—	—
rs6719884	2:59,036,916	A/C	intron variant	—
rs186770769	2:59,049,405	C/A	intron variant	—
rs17552189	2:59,072,969	C/T	intron variant	—
rs190858158	2:59,128,497	A/G	intron variant	—
rs12328778	2:59,150,956	C/T	regulatory region variant	—
rs1079815	2:59,167,905	C/A	—	—
rs111835151	2:59,202,029	G/T	—	—
rs991964	2:59,282,591	T/C	intron variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.