List of variants in gene SERPINB6 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_004568.6(SERPINB6):c.314C>A (p.Ser105Tyr)	rs148530934	0.00051
NM_004568.6(SERPINB6):c.431-12T>G	rs370453956	0.00019
NM_004568.6(SERPINB6):c.313-5C>G	rs370994947	0.00018
NM_004568.6(SERPINB6):c.946G>A (p.Val316Met)	rs550855004	0.00011
NM_004568.6(SERPINB6):c.58G>C (p.Gly20Arg)	rs775408746	0.00002
NM_004568.6(SERPINB6):c.845T>C (p.Met282Thr)	rs374321672	0.00002
NM_004568.6(SERPINB6):c.-3A>G	rs779093042
NM_004568.6(SERPINB6):c.1042C>T (p.Arg348Cys)	rs774270238
NM_004568.6(SERPINB6):c.251C>T (p.Thr84Met)	rs538616923
NM_004568.6(SERPINB6):c.383A>G (p.Glu128Gly)	rs1329989490
NM_004568.6(SERPINB6):c.503A>G (p.Tyr168Cys)	rs876657997

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