ClinVar Miner

List of variants in gene combination LDB3, LOC110121486 reported as benign

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_007078.3(LDB3):c.689+3825G>C rs3740345 0.66820
NM_007078.3(LDB3):c.690-5020A>T rs1578895 0.62980
NM_007078.3(LDB3):c.689+4181C>T rs3802662 0.57883
NM_007078.3(LDB3):c.690-5009T>C rs73344172 0.08333
NM_007078.3(LDB3):c.689+5015A>G rs113972163 0.08279
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.690-4476C>T rs78200082 0.05200
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.390G>A (p.Ser130=) rs568549202 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_001368067.1(LDB3):c.519G>A (p.Gln173=) rs537783577
NM_007078.3(LDB3):c.689+5016_689+5018dup rs3086887
NM_007078.3(LDB3):c.689+5017_689+5018dup rs3086887
NM_007078.3(LDB3):c.689+5018del rs3086887
NM_007078.3(LDB3):c.689+5018dup rs3086887
NM_007078.3(LDB3):c.690-4571A>C rs111941601
NM_007078.3(LDB3):c.690-4837C>T rs528725791

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