ClinVar Miner

List of variants in gene combination ABCG5, DYNC2LI1 reported as benign for not provided

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_022436.3(ABCG5):c.*380T>G rs2278356 0.42073
NM_022436.3(ABCG5):c.1324+164C>T rs4148187 0.36244
NM_022436.3(ABCG5):c.502-192C>T rs4557032 0.33123
NM_016008.4(DYNC2LI1):c.994-44A>G rs4952683 0.26075
NM_016008.4(DYNC2LI1):c.994-155A>G rs4953018 0.24320
NM_022436.3(ABCG5):c.*622C>T rs4148195 0.24225
NM_016008.4(DYNC2LI1):c.*16T>C rs10186552 0.23893
NM_022436.3(ABCG5):c.*416G>A rs2278357 0.21979
NM_022436.3(ABCG5):c.1810C>G (p.Gln604Glu) rs6720173 0.21159
NM_016008.4(DYNC2LI1):c.*7T>C rs8302 0.19727
NM_022436.3(ABCG5):c.*522G>A rs77105521 0.18100
NM_022436.3(ABCG5):c.502-133G>A rs17031687 0.08020
NM_022436.3(ABCG5):c.904+138T>A rs72873579 0.04839
NM_022436.3(ABCG5):c.775-259G>A rs79964831 0.04187
NM_022436.3(ABCG5):c.1650-166A>C rs74424483 0.02308
NM_016008.4(DYNC2LI1):c.*141T>G rs17031643 0.02255
NM_022436.3(ABCG5):c.1763-210T>C rs17031655 0.02252
NM_022436.3(ABCG5):c.1763-114C>G rs17031651 0.02250
NM_022436.3(ABCG5):c.1762+337G>A rs114098567 0.02248
NM_022436.3(ABCG5):c.1463+287A>C rs116594700 0.01899
NM_022436.3(ABCG5):c.1464-108A>T rs56400511 0.01800
NM_022436.3(ABCG5):c.785A>G (p.Lys262Arg) rs78070897 0.01647
NM_022436.3(ABCG5):c.1864A>G (p.Met622Val) rs140374206 0.00461
NM_022436.3(ABCG5):c.1806C>T (p.Phe602=) rs150716811 0.00052
NM_016008.4(DYNC2LI1):c.1042G>C (p.Glu348Gln) rs41281457
NM_022436.3(ABCG5):c.1463+141G>A rs55680582
NM_022436.3(ABCG5):c.1463+317_1463+318insC rs57240390
NM_022436.3(ABCG5):c.1463+318del rs55983843
NM_022436.3(ABCG5):c.1463+318dup rs55983843
NM_022436.3(ABCG5):c.1463+319C>G rs7423086
NM_022436.3(ABCG5):c.1463+319_1463+320insGG rs397781046
NM_022436.3(ABCG5):c.1463+320del rs199920905
NM_022436.3(ABCG5):c.1463+64G>A rs4073237
NM_022436.3(ABCG5):c.1464-291G>A rs4148189
NM_022436.3(ABCG5):c.634+131C>T rs56266464
NM_022436.3(ABCG5):c.775-45G>T rs111587587

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