List of variants in gene GNE reported as benign for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
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.*1781G>A	rs16933086	0.17302
NM_005476.7(GNE):c.1817-81G>C	rs2296817	0.15990
NM_005476.7(GNE):c.*1826G>C	rs7044157	0.10230
NM_005476.7(GNE):c.*630C>T	rs150102934	0.03992
NM_005476.7(GNE):c.600C>T (p.Ile200=)	rs7047950	0.02902
NM_005476.7(GNE):c.*1054C>A	rs7048468	0.01927
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.*1068A>T	rs187875852	0.00423
NM_005476.7(GNE):c.624T>G (p.Asp208Glu)	rs35224402	0.00389
NM_005476.7(GNE):c.1872G>A (p.Ala624=)	rs145361930	0.00126
NM_001128227.3(GNE):c.51+17T>G	rs144416128	0.00014
NM_005476.7(GNE):c.*2156G>C	rs2741725
NM_005476.7(GNE):c.*2196dup	rs199874473
NM_005476.7(GNE):c.*936C>T	rs56974443
NM_005476.7(GNE):c.1633+17dup

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