List of variants in gene GCM2 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: 35

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HGVS	dbSNP	gnomAD frequency
NM_004752.4(GCM2):c.91-242A>G	rs9379881	0.38078
NM_004752.4(GCM2):c.583-72A>T	rs2076257	0.35598
NM_004752.4(GCM2):c.582+88G>A	rs2076258	0.35593
NM_004752.4(GCM2):c.-44T>C	rs16870746	0.17796
NM_004752.4(GCM2):c.343+163G>A	rs9393726	0.14626
NM_004752.4(GCM2):c.582+221A>C	rs12201787	0.12704
NM_004752.4(GCM2):c.91-271A>G	rs12205626	0.11330
NM_004752.4(GCM2):c.344-290A>G	rs10456046	0.11310
NM_004752.4(GCM2):c.344-82T>G	rs77553138	0.03755
NM_004752.4(GCM2):c.344-189T>A	rs9295693	0.03179
NM_004752.4(GCM2):c.607G>A (p.Gly203Ser)	rs7744163	0.03045
NM_004752.4(GCM2):c.462G>A (p.Lys154=)	rs61734276	0.03037
NM_004752.4(GCM2):c.583-96G>A	rs6906344	0.02178
NM_004752.4(GCM2):c.897T>C (p.Pro299=)	rs73440491	0.01873
NM_004752.4(GCM2):c.91-130T>C	rs73723605	0.01510
NM_004752.4(GCM2):c.1060A>G (p.Met354Val)	rs61734278	0.01292
NM_004752.4(GCM2):c.844T>G (p.Tyr282Asp)	rs61734277	0.00874
NM_004752.4(GCM2):c.679A>G (p.Ile227Val)	rs35395043	0.00864
NM_004752.4(GCM2):c.903C>T (p.Asp301=)	rs77910271	0.00552
NM_004752.4(GCM2):c.350C>T (p.Ala117Val)	rs35786951	0.00381
NM_004752.4(GCM2):c.943A>G (p.Asn315Asp)	rs114070356	0.00258
NM_004752.4(GCM2):c.306G>A (p.Arg102=)	rs149143032	0.00142
NM_004752.4(GCM2):c.186C>T (p.Ser62=)	rs141006427	0.00026
NM_004752.3(GCM2):c.-74C>T	rs2153156
NM_004752.4(GCM2):c.1149CAC[5] (p.Thr387_Lys388insThr)
NM_004752.4(GCM2):c.583-11C>T
NM_004752.4(GCM2):c.90+135_90+152del	rs796277373
NM_004752.4(GCM2):c.90+143_90+152del	rs1230633424
NM_004752.4(GCM2):c.90+53G>A	rs79994101
NM_004752.4(GCM2):c.90+98CA[17]	rs35911329
NM_004752.4(GCM2):c.90+98CA[22]	rs35911329
NM_004752.4(GCM2):c.90+98CA[23]	rs35911329
NM_004752.4(GCM2):c.90+98CA[24]	rs35911329
NM_004752.4(GCM2):c.90+98CA[25]	rs35911329
NM_004752.4(GCM2):c.91-11C>T

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