ClinVar Miner

List of variants in gene LRBA reported as uncertain significance by Baylor Genetics

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001364905.1(LRBA):c.1399A>G (p.Met467Val) rs116355217 0.00225
NM_001364905.1(LRBA):c.194T>C (p.Ile65Thr) rs148385798 0.00205
NM_001364905.1(LRBA):c.5754+15T>C rs112952572 0.00118
NM_001364905.1(LRBA):c.5744C>T (p.Ala1915Val) rs201500267 0.00019
NM_001364905.1(LRBA):c.5899G>A (p.Ala1967Thr) rs141395658 0.00010
NM_001364905.1(LRBA):c.2671T>C (p.Tyr891His) rs757344529 0.00007
NM_001364905.1(LRBA):c.5470C>T (p.Arg1824Trp) rs374719524 0.00005
NM_001364905.1(LRBA):c.2504G>A (p.Ser835Asn) rs866363880 0.00004
NM_001364905.1(LRBA):c.637A>G (p.Ser213Gly) rs538370042 0.00004
NM_001364905.1(LRBA):c.782A>G (p.Lys261Arg) rs375175981 0.00002
NM_001364905.1(LRBA):c.3263A>G (p.Glu1088Gly) rs1387505849 0.00001
NM_001364905.1(LRBA):c.4186C>G (p.Gln1396Glu) rs760112656 0.00001
NM_001364905.1(LRBA):c.4618A>C (p.Ile1540Leu) rs550389924 0.00001
NM_001364905.1(LRBA):c.5401G>A (p.Glu1801Lys) rs199596976 0.00001
NM_001364905.1(LRBA):c.1937C>G (p.Pro646Arg) rs755987682
NM_001364905.1(LRBA):c.3826-13A>G rs1750538092
NM_001364905.1(LRBA):c.6223C>T (p.Leu2075Phe) rs1772352730
NM_001364905.1(LRBA):c.6994A>G (p.Ile2332Val)

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