List of variants in gene ADGRG1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_201525.4(ADGRG1):c.996T>C (p.Thr332=)	rs1376041	0.79529
NM_201525.4(ADGRG1):c.*38T>G	rs10852554	0.76824
NM_201525.4(ADGRG1):c.1168-20C>A	rs2305309	0.37206
NM_201525.4(ADGRG1):c.1665-5C>T	rs2290177	0.20927
NM_201525.4(ADGRG1):c.918A>C (p.Gln306His)	rs1801255	0.20047
NM_201525.4(ADGRG1):c.1286+6G>A	rs74326170	0.05376
NM_201525.4(ADGRG1):c.*19C>A	rs74022020	0.03705
NM_201525.4(ADGRG1):c.1460T>C (p.Met487Thr)	rs17379472	0.02860
NM_201525.4(ADGRG1):c.1555+15G>C	rs75843478	0.01900
NM_201525.4(ADGRG1):c.236G>A (p.Arg79Gln)	rs13338340	0.00481
NM_201525.4(ADGRG1):c.1933+10A>G	rs137936275	0.00438
NM_201525.4(ADGRG1):c.844G>C (p.Gly282Arg)	rs146704802	0.00404
NM_201525.4(ADGRG1):c.1017+8G>A	rs186479054	0.00196
NM_201525.4(ADGRG1):c.1287-28G>C	rs60624815	0.00163
NM_201525.4(ADGRG1):c.132C>T (p.Ser44=)	rs12599906	0.00034
NM_201525.4(ADGRG1):c.1665-41C>T	rs17240890
NM_201525.4(ADGRG1):c.843C>G (p.Ser281Arg)	rs1801257

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