List of variants in gene SCP2 reported as likely benign by GeneDx

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_002979.5(SCP2):c.674+181A>G	rs12568454	0.02696
NC_000001.11:g.52926925G>T	rs28384398	0.02377
NM_002979.5(SCP2):c.70-278_70-277insCT	rs772407457	0.01402
NM_002979.5(SCP2):c.70-277A>G	rs759019329	0.01321
NM_002979.5(SCP2):c.1236-172C>T	rs138484563	0.00826
NM_002979.5(SCP2):c.*56A>G	rs74363442	0.00781
NM_002979.5(SCP2):c.332-184G>T	rs78958884	0.00764
NM_002979.5(SCP2):c.1469-142A>G	rs77330664	0.00704
NM_002979.5(SCP2):c.1081+5248G>A	rs117140349	0.00694
NM_002979.5(SCP2):c.1236-210C>T	rs13376704	0.00680
NM_002979.5(SCP2):c.1468+229T>G	rs79434090	0.00655
NM_002979.5(SCP2):c.1081+214A>G	rs150407225	0.00632
NM_002979.5(SCP2):c.1235+154C>T	rs111837528	0.00631
NM_002979.5(SCP2):c.1224G>A (p.Pro408=)	rs80253221	0.00630
NM_002979.5(SCP2):c.127+63A>G	rs78381436	0.00610
NM_002979.5(SCP2):c.973+312C>T	rs140753873	0.00570
NM_002979.5(SCP2):c.1548+186C>T	rs11206080	0.00414
NM_002979.5(SCP2):c.1338+89T>C	rs142918339	0.00303
NM_002979.5(SCP2):c.675-6T>C	rs115815213	0.00289
NM_002979.5(SCP2):c.1081+5247C>T	rs182127561	0.00226
NM_002979.5(SCP2):c.1468+17C>A	rs79342751	0.00163
NM_002979.5(SCP2):c.332-23A>G	rs376418700	0.00126
NM_002979.5(SCP2):c.70-46T>A	rs752790329	0.00089
NM_002979.5(SCP2):c.397-34C>G	rs139280584	0.00065
NM_002979.5(SCP2):c.200-45C>G	rs12041343	0.00036
NM_002979.5(SCP2):c.1339-266C>A	rs190205544
NM_002979.5(SCP2):c.674+286G>A	rs74547030
NM_002979.5(SCP2):c.675-237dup	rs57875662
NM_002979.5(SCP2):c.70-47dup	rs143386725
NM_002979.5(SCP2):c.70-48_70-47dup	rs143386725
NM_002979.5(SCP2):c.973+151G>A	rs116807594

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