List of variants in gene CHRNG reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_005199.5(CHRNG):c.921-56C>G	rs2573206	0.83377
NM_005199.5(CHRNG):c.507-135T>G	rs1881492	0.80934
NM_005199.5(CHRNG):c.604+181T>A	rs6761667	0.45151
NM_005199.5(CHRNG):c.605-76G>C	rs2697782	0.35626
NM_005199.5(CHRNG):c.351-254G>T	rs13003665	0.31177
NM_005199.5(CHRNG):c.55+78G>C	rs12996322	0.30905
NM_005199.5(CHRNG):c.921-12C>T	rs13018423	0.22363
NM_005199.5(CHRNG):c.350+229G>A	rs67583510	0.20419
NM_005199.5(CHRNG):c.507-13C>T	rs2853462	0.20060
NM_005199.5(CHRNG):c.1035+105A>T	rs72991926	0.17672
NM_005199.5(CHRNG):c.1035+49C>T	rs73995686	0.02252
NM_005199.5(CHRNG):c.1035+64C>T	rs57945834	0.01662
NC_000002.12:g.232539584C>G	rs11674608
NC_000002.12:g.232539628CTGGCTGGG[3]	rs59498978
NM_005199.5(CHRNG):c.351-278TAT[5]	rs202064405
NM_005199.5(CHRNG):c.605-10_605-3dup	rs202023568
NM_005199.5(CHRNG):c.920+97_921-97dup	rs34697564
NM_005199.5(CHRNG):c.921-68del	rs10714586
NM_005199.5(CHRNG):c.921-97del	rs34697564
NM_005199.5(CHRNG):c.921-97dup	rs34697564

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