ClinVar Miner

List of variants reported as benign for Intellectual disability, X-linked 21

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_014271.4(IL1RAPL1):c.-19G>A rs6526806 0.61514
NM_014271.4(IL1RAPL1):c.-39G>A rs143054072 0.00962
NM_014271.4(IL1RAPL1):c.1191G>A (p.Glu397=) rs7049358 0.00631
NM_014271.4(IL1RAPL1):c.1605G>T (p.Thr535=) rs35305747 0.00223
NM_014271.4(IL1RAPL1):c.36C>T (p.Tyr12=) rs148060509 0.00132
NM_014271.4(IL1RAPL1):c.12G>A (p.Pro4=) rs143600441 0.00127
NM_014271.4(IL1RAPL1):c.2067C>G (p.Thr689=) rs140330609 0.00111
NM_014271.4(IL1RAPL1):c.-20C>T rs200878713 0.00072
NM_014271.4(IL1RAPL1):c.83-6C>T rs180930821 0.00066
NM_014271.4(IL1RAPL1):c.1136A>G (p.Lys379Arg) rs138267399 0.00036
NM_014271.4(IL1RAPL1):c.550-4A>G rs368301683 0.00008
NM_014271.4(IL1RAPL1):c.1443C>T (p.Tyr481=) rs777536426 0.00006
NM_014271.4(IL1RAPL1):c.726C>A (p.Pro242=) rs748193306 0.00006
NM_014271.4(IL1RAPL1):c.-25+14A>C rs146138116 0.00005
NM_014271.4(IL1RAPL1):c.1089C>T (p.Gly363=) rs201215945 0.00001

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