List of variants in gene LDB3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.690-4A>G	rs45529531	0.00427
NM_007078.3(LDB3):c.147G>A (p.Val49=)	rs45591834	0.00312
NM_007078.3(LDB3):c.2016C>T (p.Cys672=)	rs45578640	0.00288
NM_007078.3(LDB3):c.-23-32C>A	rs34972863	0.00282
NM_007078.3(LDB3):c.1422G>A (p.Ser474=)	rs142625982	0.00136
NM_007078.3(LDB3):c.897-6834C>T	rs185972751	0.00101
NM_007078.3(LDB3):c.1653C>T (p.Cys551=)	rs45581435	0.00096
NM_007078.3(LDB3):c.993G>A (p.Ala331=)	rs140347820	0.00095
NM_007078.3(LDB3):c.1535A>C (p.Gln512Pro)	rs138951890	0.00080
NM_001368067.1(LDB3):c.780C>T (p.Asn260=)	rs372789789	0.00061
NM_007078.3(LDB3):c.1594G>C (p.Ala532Pro)	rs143764931	0.00036
NM_007078.3(LDB3):c.1035C>T (p.Ile345=)	rs121908336	0.00029
NM_007078.3(LDB3):c.1051A>G (p.Thr351Ala)	rs138251566	0.00026
NM_007078.3(LDB3):c.1956C>T (p.Asp652=)	rs139213290	0.00013
NM_007078.3(LDB3):c.1254G>A (p.Pro418=)	rs145942370	0.00006
NM_001368067.1(LDB3):c.770C>T (p.Thr257Met)	rs375798002	0.00004
NM_007078.3(LDB3):c.944C>T (p.Pro315Leu)	rs371649487	0.00004
NM_007078.3(LDB3):c.1672A>G (p.Ile558Val)	rs372331627	0.00003
NM_007078.3(LDB3):c.2124G>A (p.Pro708=)	rs759812655	0.00002
NM_001368063.1(LDB3):c.-35G>T
NM_007078.3(LDB3):c.1317C>T (p.Pro439=)	rs397517208
NM_007078.3(LDB3):c.1538C>A (p.Thr513Asn)	rs748433510
NM_007078.3(LDB3):c.465C>T (p.Leu155=)	rs45516997

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