ClinVar Miner

List of variants reported as likely benign for Intellectual disability, autosomal recessive 47

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_020066.5(FMN2):c.2897T>C (p.Leu966Pro) rs200975594 0.04768
NM_020066.5(FMN2):c.2886A>G (p.Ala962=) rs199866405 0.00564
NM_020066.5(FMN2):c.1259A>C (p.Lys420Thr) rs146681532 0.00336
NM_020066.5(FMN2):c.5136T>G (p.Ser1712=) rs143796494 0.00321
NM_020066.5(FMN2):c.2844_2876del (p.Ala952_Ala962del) rs758726356
NM_020066.5(FMN2):c.2888_2889insAATACCTCCTCCACCCCCTCTACCCGGAGCGGG (p.Pro965_Leu966insProProProProLeuProGlyAlaGlyIlePro)
NM_020066.5(FMN2):c.2984_2985insAGGAATACCTCCTCCACCCCCTCTACCCGGAGC (p.Gly1104_Val1105insAlaGlyIleProProProProProLeuProGly)
NM_020066.5(FMN2):c.3324TCC[1] (p.Pro1112del) rs780903069
NM_020066.5(FMN2):c.3442_3507del (p.Arg1148_Pro1169del) rs1558365026

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