ClinVar Miner

List of variants in gene MED17 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_004268.5(MED17):c.859+18T>C rs657177 0.94089
NC_000011.10:g.93783896A>G rs653934 0.93776
NM_004268.5(MED17):c.638-316T>C rs670391 0.80822
NM_004268.5(MED17):c.1013-142T>C rs687042 0.77757
NM_004268.5(MED17):c.1329-70_1329-69del rs879652942 0.77703
NM_004268.5(MED17):c.1329-72_1329-71insGA rs530877628 0.77677
NM_004268.5(MED17):c.417+72C>T rs676586 0.74792
NM_004268.5(MED17):c.1329-11G>A rs655699 0.52298
NM_004268.5(MED17):c.859+232C>G rs685865 0.21575
NM_004268.5(MED17):c.1466+175C>G rs10831103 0.21357
NM_004268.5(MED17):c.1584+113T>G rs72978409 0.21345
NM_004268.5(MED17):c.1329-71T>G rs35544640 0.16934
NM_004268.5(MED17):c.1092G>A (p.Pro364=) rs34057693 0.11341
NM_004268.5(MED17):c.1466+315A>G rs55734929 0.09683
NM_004268.5(MED17):c.637+165A>C rs61628694 0.06063
NM_004268.5(MED17):c.637+87T>G rs7108692 0.05537
NM_004268.5(MED17):c.342T>C (p.Asp114=) rs16919376 0.05535
NM_004268.5(MED17):c.516C>T (p.Thr172=) rs7119915 0.05273
NM_004268.5(MED17):c.1012+283T>C rs79017912 0.05134
NM_004268.5(MED17):c.1548T>C (p.Tyr516=) rs16919389 0.04169
NM_004268.5(MED17):c.1260A>G (p.Ser420=) rs36120755 0.03633
NM_004268.5(MED17):c.1467-333G>A rs140630862 0.03133
NM_004268.5(MED17):c.1467-176A>G rs150481911 0.02400
NM_004268.5(MED17):c.1467-127dup rs140127665 0.02222
NM_004268.5(MED17):c.1585-169G>A rs78581292 0.02220
NM_004268.5(MED17):c.1585-71C>T rs77602634 0.02220
NM_004268.5(MED17):c.1744+303del rs143412294 0.02220
NM_004268.5(MED17):c.1328+12G>A rs16919387 0.02219
NM_004268.5(MED17):c.1143+203G>T rs16919384 0.01732
NM_004268.5(MED17):c.690C>T (p.Leu230=) rs116727804 0.00467
NM_004268.5(MED17):c.978G>C (p.Val326=) rs2276311 0.00357
NM_004268.5(MED17):c.1328+150G>A rs56893874
NM_004268.5(MED17):c.1329-70T>A rs34875966
NM_004268.5(MED17):c.638-202del rs369708342
NM_004268.5(MED17):c.638-202dup rs369708342
NM_004268.5(MED17):c.859+185_859+186dup rs35300764
NM_004268.5(MED17):c.859+87del rs5793656

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