List of variants in gene GCKR reported as benign for not provided

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001486.4(GCKR):c.1337T>C (p.Leu446Pro)	rs1260326	0.67353
NM_001486.4(GCKR):c.429-38T>C	rs813592	0.47481
NM_001486.4(GCKR):c.549+99G>A	rs1260320	0.44737
NM_001486.4(GCKR):c.968+34G>A	rs2293571	0.38718
NM_001486.4(GCKR):c.869+74C>G	rs2293572	0.38671
NM_001486.4(GCKR):c.1422+258C>T	rs35073769	0.37937
NM_001486.4(GCKR):c.1708-190A>G	rs7589217	0.36453
NM_001486.4(GCKR):c.1422+94T>C	rs3817588	0.14182
NM_001486.4(GCKR):c.217-44C>T	rs8179205	0.07623
NM_001486.4(GCKR):c.1241-27G>A	rs8179219	0.06335
NM_001486.4(GCKR):c.*104G>A	rs704790	0.04118
NM_001486.4(GCKR):c.1423-22C>G	rs8179236	0.03975
NM_001486.4(GCKR):c.354+132C>G	rs4270306	0.03847
NM_001486.4(GCKR):c.1619G>A (p.Arg540Gln)	rs8179249	0.00435
NM_001486.4(GCKR):c.244A>G (p.Thr82Ala)	rs116837855	0.00203
NM_001486.4(GCKR):c.1215T>C (p.Thr405=)	rs140213973	0.00169
NM_001486.4(GCKR):c.307G>A (p.Val103Met)	rs146175795	0.00151
NM_001486.4(GCKR):c.474C>T (p.His158=)	rs8179207	0.00086
NM_001486.4(GCKR):c.822A>G (p.Leu274=)	rs61734462	0.00076
NM_001486.4(GCKR):c.230A>G (p.Glu77Gly)	rs8179206	0.00069
NM_001486.4(GCKR):c.354G>A (p.Ser118=)	rs143881585	0.00039
NM_001486.4(GCKR):c.1501C>T (p.Leu501=)	rs537585051	0.00031
NM_001486.4(GCKR):c.152G>A (p.Arg51Gln)
NM_001486.4(GCKR):c.1581T>C (p.Ser527=)
NM_001486.4(GCKR):c.1756G>T (p.Glu586Ter)
NM_001486.4(GCKR):c.189G>A (p.Glu63=)
NM_001486.4(GCKR):c.216+9_216+10del	rs57332022

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