List of variants in gene ADGRG1 reported as likely benign for congenital nervous system disorder

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_201525.4(ADGRG1):c.1460T>C (p.Met487Thr)	rs17379472	0.02860
NM_201525.4(ADGRG1):c.844G>C (p.Gly282Arg)	rs146704802	0.00404
NM_201525.4(ADGRG1):c.*46G>A	rs201611287	0.00217
NM_201525.4(ADGRG1):c.174C>T (p.Ile58=)	rs140963173	0.00217
NM_201525.4(ADGRG1):c.1017+8G>A	rs186479054	0.00196
NM_201525.4(ADGRG1):c.*1058C>T	rs149861292	0.00164
NM_201525.4(ADGRG1):c.1983T>C (p.Gly661=)	rs111939130	0.00113
NM_201525.4(ADGRG1):c.*189G>T	rs184796447	0.00062
NM_005682.7(ADGRG1):c.-227C>A	rs549770392	0.00048
NM_201525.4(ADGRG1):c.1188C>T (p.Asp396=)	rs368883473	0.00014
NM_201525.4(ADGRG1):c.1287-6G>A	rs112805221	0.00014
NM_201525.4(ADGRG1):c.1647C>T (p.Gly549=)	rs2278808	0.00014
NM_201525.4(ADGRG1):c.801G>C (p.Val267=)	rs141056936	0.00006
NM_201525.4(ADGRG1):c.1491C>T (p.Leu497=)	rs369114425	0.00005
NM_201525.4(ADGRG1):c.1146G>A (p.Leu382=)	rs770806177	0.00003
NM_201525.4(ADGRG1):c.246T>C (p.Pro82=)	rs768452683	0.00003
NM_201525.4(ADGRG1):c.1143C>T (p.His381=)	rs746825547	0.00001
NM_201525.4(ADGRG1):c.1200G>A (p.Lys400=)	rs760911899	0.00001
NM_201525.4(ADGRG1):c.1236C>T (p.Val412=)	rs768769972	0.00001
NM_201525.4(ADGRG1):c.1560C>T (p.Phe520=)	rs548451753	0.00001
NM_201525.4(ADGRG1):c.2049G>A (p.Ser683=)	rs771915499	0.00001
NM_201525.4(ADGRG1):c.553C>T (p.Leu185=)	rs138495764	0.00001
NM_201525.4(ADGRG1):c.831G>A (p.Thr277=)	rs552642182	0.00001
NM_201525.4(ADGRG1):c.*304C>A	rs35572780
NM_201525.4(ADGRG1):c.-35-8595C>T	rs151010444
NM_201525.4(ADGRG1):c.1978C>A (p.Arg660=)	rs777803292
NM_201525.4(ADGRG1):c.462C>T (p.Ala154=)	rs373133040
NM_201525.4(ADGRG1):c.840G>A (p.Arg280=)	rs1597552134

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