List of variants in gene combination LDB3, LOC110121486 reported as likely benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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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_007078.3(LDB3):c.690-4345G>A	rs117280687	0.01754
NM_001368067.1(LDB3):c.349G>A (p.Asp117Asn)	rs121908338	0.00584
NM_007078.3(LDB3):c.689+4041G>A	rs73344165	0.00573
NM_007078.3(LDB3):c.690-4896C>G	rs113616598	0.00485
NM_001368067.1(LDB3):c.546T>C (p.Ser182=)	rs71473272	0.00316
NM_007078.3(LDB3):c.690-4621A>G	rs370053163	0.00016
NM_001368067.1(LDB3):c.511G>A (p.Ala171Thr)	rs373632943	0.00015
NM_001368067.1(LDB3):c.393C>T (p.Ala131=)	rs368832031	0.00013
NM_001368067.1(LDB3):c.415G>A (p.Glu139Lys)	rs374613600	0.00006
NM_001368067.1(LDB3):c.346G>A (p.Ala116Thr)	rs200458194	0.00005
NM_001368067.1(LDB3):c.348C>T (p.Ala116=)	rs397516557	0.00004
NM_007078.3(LDB3):c.689+3861C>T	rs754704023	0.00004
NM_007078.3(LDB3):c.690-4616C>T	rs757618215	0.00001
NM_001368067.1(LDB3):c.468G>A (p.Thr156=)	rs745413406
NM_007078.3(LDB3):c.690-4837C>T	rs528725791

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