List of variants in gene SPPL2A 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_032802.4(SPPL2A):c.376A>G (p.Asn126Asp)	rs61751063	0.02112
NM_032802.4(SPPL2A):c.1035C>G (p.Gly345=)	rs76947817	0.01749
NM_032802.4(SPPL2A):c.1090-4T>G	rs118053549	0.01189
NM_032802.4(SPPL2A):c.1424C>G (p.Thr475Ser)	rs145209254	0.00950
NM_032802.4(SPPL2A):c.1179C>A (p.Ile393=)	rs140457962	0.00600
NM_032802.4(SPPL2A):c.1015-17G>A	rs114940488	0.00463
NM_032802.4(SPPL2A):c.1554C>G (p.Val518=)	rs146593203	0.00142
NM_032802.4(SPPL2A):c.101G>A (p.Gly34Glu)	rs145832874	0.00117
NM_032802.4(SPPL2A):c.450+17A>G	rs201316053	0.00074
NM_032802.4(SPPL2A):c.1327+12T>C	rs199712140	0.00032
NM_032802.4(SPPL2A):c.1147-37GTTTT[4]	rs140174698
NM_032802.4(SPPL2A):c.1147-37GTTTT[5]	rs140174698
NM_032802.4(SPPL2A):c.1147-37GTTTT[7]	rs140174698
NM_032802.4(SPPL2A):c.734-4dup
NM_032802.4(SPPL2A):c.933-3dup	rs2141036273

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