ClinVar Miner

List of variants reported by Research Lab, National Institute of Public Health

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_004996.4(ABCC1):c.2292+288G>A rs11075295 0.83985
NM_004996.4(ABCC1):c.1913-617C>T rs35625 0.60093
NM_003981.4(PRC1):c.1792-828T>C rs12910825 0.56832
NM_003981.4(PRC1):c.1350+35C>G rs12898311 0.52787
NM_003981.4(PRC1):c.*769A>G rs7601 0.46627
NM_004996.4(ABCC1):c.1988+357G>T rs35626 0.40581
NM_003981.4(PRC1):c.970+436G>A rs6496742 0.39225
NM_003981.4(PRC1):c.12-2765T>C rs8028856 0.38070
NM_003981.4(PRC1):c.282G>A (p.Thr94=) rs2301826 0.37356
NM_003981.4(PRC1):c.145-81A>T rs8031684 0.32249
NM_004996.4(ABCC1):c.2461-1217G>A rs3888565 0.25007
NM_003981.4(PRC1):c.268-107G>A rs11857612 0.15952
NM_004996.4(ABCC1):c.1913-718G>T rs35623 0.14934
NM_003981.4(PRC1):c.268-203A>G rs11855081 0.12736
NM_004996.4(ABCC1):c.1988+848A>G rs35628 0.12670
NM_004996.4(ABCC1):c.1988+890G>T rs4148353 0.10946
NM_003981.4(PRC1):c.1462-1016G>A rs11852999 0.10280
NM_003981.4(PRC1):c.1351-3C>T rs17636091 0.09389
NM_003981.4(PRC1):c.971-442C>T rs10520699 0.08779
NM_003981.4(PRC1):c.*627T>C rs14280 0.08057
NM_004996.4(ABCC1):c.1988+219G>T rs4148350 0.07631
NM_003981.4(PRC1):c.*441C>A rs3743450 0.05570
NM_003981.4(PRC1):c.1532A>G (p.Tyr511Cys) rs12911192 0.04874
NM_003981.4(PRC1):c.*919G>T rs15172 0.04817
NM_004996.4(ABCC1):c.2168G>A (p.Arg723Gln) rs4148356 0.01253
NM_003981.4(PRC1):c.971-441G>A rs59025289 0.00503
NM_003981.4(PRC1):c.*342A>G rs112187198 0.00059
NM_003981.4(PRC1):c.*733G>A rs112770009 0.00025
NM_003981.4(PRC1):c.971-466T>C rs190852637 0.00002
NM_003981.4(PRC1):c.971-375A>G rs186031385 0.00001
NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266
NM_004996.4(ABCC1):c.1913-609G>A rs11866794
NM_004996.4(ABCC1):c.1988+310C>T rs4148351
NM_004996.4(ABCC1):c.2461-1175C>G rs3851711

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