List of variants in gene combination LDB3, LOC110121486 reported 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
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001368067.1(LDB3):c.504T>C (p.Asp168=)	rs76615432	0.06909
NM_007078.3(LDB3):c.690-4842G>A	rs113445294	0.06823
NM_001368067.1(LDB3):c.349G>A (p.Asp117Asn)	rs121908338	0.00584
NM_001368067.1(LDB3):c.546T>C (p.Ser182=)	rs71473272	0.00316
NM_001368067.1(LDB3):c.511G>A (p.Ala171Thr)	rs373632943	0.00015
NM_001368067.1(LDB3):c.415G>A (p.Glu139Lys)	rs374613600	0.00006
NM_001368067.1(LDB3):c.348C>T (p.Ala116=)	rs397516557	0.00004
NM_007078.3(LDB3):c.689+3861C>T	rs754704023	0.00004
NM_001368067.1(LDB3):c.456G>A (p.Ala152=)	rs371708921	0.00002
NM_007078.3(LDB3):c.690-4832C>T	rs546887989	0.00001
NM_001368067.1(LDB3):c.324G>T (p.Val108=)	rs397516556
NM_001368067.1(LDB3):c.327A>G (p.Val109=)	rs876657489
NM_001368067.1(LDB3):c.456G>T (p.Ala152=)	rs371708921
NM_001368067.1(LDB3):c.494C>T (p.Ala165Val)	rs121908334
NM_007078.3(LDB3):c.690-4842G>T	rs113445294

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