ClinVar Miner

List of variants in gene GNE reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_005476.7(GNE):c.1933+162G>C rs615108 0.80967
NM_001128227.3(GNE):c.51+34T>C rs7875447 0.75717
NM_005476.7(GNE):c.*2391C>T rs1043313 0.71766
NM_005476.7(GNE):c.165-115A>G rs7861442 0.50498
NM_005476.7(GNE):c.1282-302G>A rs28576111 0.48653
NM_005476.7(GNE):c.1934-201C>T rs616009 0.42970
NM_005476.7(GNE):c.1282-155C>T rs10758350 0.30335
NM_001128227.3(GNE):c.52-9153G>A rs35078360 0.17375
NM_005476.7(GNE):c.*1781G>A rs16933086 0.17302
NM_005476.7(GNE):c.1817-81G>C rs2296817 0.15990
NM_005476.7(GNE):c.982+247T>G rs202137023 0.11498
NM_005476.7(GNE):c.1633+125G>C rs10972795 0.09219
NM_005476.7(GNE):c.1634-117A>G rs2296818 0.09084
NM_005476.7(GNE):c.616+269T>C rs7871216 0.08144
NM_005476.7(GNE):c.1633+237C>T rs11793464 0.08058
NM_005476.7(GNE):c.-42-248C>T rs185612372 0.06896
NM_001128227.2(GNE):c.-230G>A rs72624019 0.06001
NM_005476.7(GNE):c.983-273G>A rs77468060 0.04525
NM_005476.7(GNE):c.1281+44G>A rs16933102 0.03050
NM_005476.7(GNE):c.617-298T>C rs16933114 0.02964
NM_005476.7(GNE):c.600C>T (p.Ile200=) rs7047950 0.02902
NM_005476.7(GNE):c.1633+118T>C rs2772222 0.01972
NM_005476.7(GNE):c.1770C>T (p.Tyr590=) rs111302956 0.01688
NM_001128227.3(GNE):c.-10G>A rs73449614 0.00894
NM_005476.7(GNE):c.624T>G (p.Asp208Glu) rs35224402 0.00389
NM_005476.7(GNE):c.1070+208dup rs71336431
NM_005476.7(GNE):c.1070+226_1070+227del rs71336431
NM_005476.7(GNE):c.1070+227del rs71336431
NM_005476.7(GNE):c.1281+50dup rs150174400
NM_005476.7(GNE):c.1282-267dup rs377239651
NM_005476.7(GNE):c.1282-281C>T rs140478304
NM_005476.7(GNE):c.165-179del rs66781293
NM_005476.7(GNE):c.982+253del rs34150061

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