List of variants in gene SP110 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_080424.4(SP110):c.1274T>C (p.Leu425Ser)	rs3948464	0.86768
NM_080424.4(SP110):c.1568T>C (p.Met523Thr)	rs1135791	0.39929
NM_080424.4(SP110):c.1815+14A>G	rs34034766	0.11238
NM_080424.4(SP110):c.1731C>T (p.Cys577=)	rs13018234	0.10366
NM_080424.4(SP110):c.1737G>A (p.Met579Ile)	rs3948463	0.05302
NM_080424.4(SP110):c.1650T>C (p.Gly550=)	rs35495464	0.05293

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