List of variants in gene GRIP1 reported as benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001366722.1(GRIP1):c.2464+15T>C	rs7970076	0.97982
NM_001366722.1(GRIP1):c.2461C>G (p.Gln821Glu)	rs13277	0.87545
NM_001366722.1(GRIP1):c.724+10G>A	rs12316942	0.67684
NM_001366722.1(GRIP1):c.1838+13G>T	rs7397862	0.49975
NM_001366722.1(GRIP1):c.*616T>C	rs1168308	0.47053
NM_001366722.1(GRIP1):c.725-19A>G	rs12820901	0.27830
NM_001366722.1(GRIP1):c.503-15C>A	rs11838180	0.27190
NM_001366722.1(GRIP1):c.418+26A>G	rs66522623	0.25360
NM_001366722.1(GRIP1):c.2606G>A (p.Arg869Gln)	rs145115262	0.00595
NM_001366722.1(GRIP1):c.2880G>A (p.Ser960=)	rs181527317	0.00242
NM_001366722.1(GRIP1):c.*428C>T	rs78619935	0.00225
NM_001366722.1(GRIP1):c.3207C>T (p.Pro1069=)	rs187691546	0.00172
NM_001366722.1(GRIP1):c.2283G>A (p.Ser761=)	rs200863167	0.00168
NM_001366722.1(GRIP1):c.1199-7C>G	rs200313638	0.00029
NM_001366722.1(GRIP1):c.692C>T (p.Ala231Val)	rs150958775	0.00029
NM_001366722.1(GRIP1):c.1687+12T>C	rs151041073	0.00023
NM_001366722.1(GRIP1):c.1688-3T>C	rs185129168	0.00021
NM_001366722.1(GRIP1):c.2327G>A (p.Gly776Glu)	rs181365280	0.00006
NM_001366722.1(GRIP1):c.3222C>T (p.Ser1074=)	rs558365010	0.00006
NM_001366722.1(GRIP1):c.1389G>A (p.Gly463=)	rs200499586	0.00002
NM_001366722.1(GRIP1):c.1354+19A>G
NM_001366722.1(GRIP1):c.1355-10_1355-8del	rs148083271
NM_001366722.1(GRIP1):c.1541+20A>G
NM_001366722.1(GRIP1):c.1687+19_1687+20insTCAAGTCAGTGACAGAG
NM_001366722.1(GRIP1):c.1787C>G (p.Pro596Arg)	rs200955760
NM_001366722.1(GRIP1):c.273-9A>G
NM_001366722.1(GRIP1):c.418+14C>A	rs79994510
NM_001366722.1(GRIP1):c.418+19dup
NM_001366722.1(GRIP1):c.502+20del
NM_001366722.1(GRIP1):c.964G>A (p.Ala322Thr)	rs17102531

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