ClinVar Miner

List of variants in gene GPC6 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_005708.5(GPC6):c.319+86315C>G rs3843688 0.78036
NM_005708.5(GPC6):c.1008+52A>G rs1409174 0.65374
NM_005708.5(GPC6):c.319+111352A>G rs9589807 0.48812
NM_005708.5(GPC6):c.319+86317G>A rs3848065 0.45340
NM_005708.5(GPC6):c.-623G>A rs319522 0.40798
NM_005708.5(GPC6):c.161-300G>A rs12854090 0.37696
NM_005708.5(GPC6):c.711+226T>C rs45608931 0.23641
NM_005708.5(GPC6):c.1289+327A>T rs4566021 0.19202
NM_005708.5(GPC6):c.1289+233T>A rs4280106 0.19088
NM_005708.5(GPC6):c.1234G>A (p.Val412Met) rs1535692 0.17631
NM_005708.5(GPC6):c.-320C>A rs17645969 0.15297
NM_005708.5(GPC6):c.877+144A>T rs9589883 0.13123
NM_005708.5(GPC6):c.1248G>A (p.Thr416=) rs2274020 0.10346
NM_005708.5(GPC6):c.1289+106G>T rs2274021 0.09693
NM_005708.5(GPC6):c.1466-133A>C rs9556370 0.08471
NM_005708.5(GPC6):c.711+86A>C rs766813934 0.07054
NM_005708.5(GPC6):c.1153-128T>C rs9524470 0.05823
NM_005708.5(GPC6):c.1289+113G>A rs9589985 0.04778
NM_005708.5(GPC6):c.319+86545G>T rs73543538 0.04537
NM_005708.5(GPC6):c.320-183A>G rs7139626 0.04242
NM_005708.5(GPC6):c.*255G>A rs9584224 0.03844
NC_000013.11:g.93226778A>G rs7985891 0.03717
NM_005708.5(GPC6):c.1290-232A>G rs79505744 0.03497
NM_005708.5(GPC6):c.319+61454A>G rs115658494 0.01890
NM_005708.5(GPC6):c.319+86342A>G rs9589799 0.01848
GRCh38/hg38 13q31.3(chr13:93689856-93770897)x3
NM_005708.5(GPC6):c.1009-134T>A rs10492630
NM_005708.5(GPC6):c.1153-313C>G rs7991005
NM_005708.5(GPC6):c.319+177del rs397851797
NM_005708.5(GPC6):c.711+91_711+93del rs369020255
NM_005708.5(GPC6):c.711+92_711+93del rs369020255
NM_005708.5(GPC6):c.711+92_711+93dup rs369020255
NM_005708.5(GPC6):c.711+93del rs369020255
NM_005708.5(GPC6):c.711+93dup rs369020255

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