ClinVar Miner

List of variants in gene LRBA reported as uncertain significance for not specified

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001364905.1(LRBA):c.2674G>A (p.Ala892Thr) rs151098394 0.00465
NM_001364905.1(LRBA):c.3350G>T (p.Gly1117Val) rs35977354 0.00462
NM_001364905.1(LRBA):c.1399A>G (p.Met467Val) rs116355217 0.00225
NM_001364905.1(LRBA):c.*9G>T rs150102345 0.00194
NM_001364905.1(LRBA):c.2637G>A (p.Lys879=) rs138956153 0.00170
NM_001364905.1(LRBA):c.8551C>T (p.Arg2851Cys) rs145709687 0.00152
NM_001364905.1(LRBA):c.3407C>T (p.Pro1136Leu) rs113022115 0.00033
NM_001364905.1(LRBA):c.3392A>G (p.Asp1131Gly) rs553138286 0.00026
NM_001364905.1(LRBA):c.3499A>G (p.Thr1167Ala) rs146297781 0.00026
NM_001364905.1(LRBA):c.6848A>T (p.Asp2283Val) rs147096866 0.00012
NM_001364905.1(LRBA):c.7021C>T (p.Arg2341Cys) rs139428686 0.00004
NM_001364905.1(LRBA):c.7177G>A (p.Val2393Ile) rs202243949 0.00004
NM_001364905.1(LRBA):c.1316A>G (p.Asn439Ser) rs572309256 0.00003
NM_001364905.1(LRBA):c.4919T>C (p.Val1640Ala) rs773862243 0.00001
NM_001364905.1(LRBA):c.6443A>G (p.Asn2148Ser) rs143949228 0.00001
NM_001364905.1(LRBA):c.7690A>G (p.Ile2564Val) rs200047974 0.00001
GRCh37/hg19 4q31.3(chr4:151668145-151830578)
NC_000004.11:g.(151656519_151682934)_(151936650_?)dup
NM_001364905.1(LRBA):c.5227A>G (p.Ser1743Gly) rs768830356
NM_001364905.1(LRBA):c.8163G>T (p.Arg2721Ser) rs1307266786

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