ClinVar Miner

List of variants reported as likely pathogenic for Pyogenic bacterial infections due to MyD88 deficiency

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002468.5(MYD88):c.103_104del (p.Leu35fs)	rs776336832
NM_002468.5(MYD88):c.154GAG[1] (p.Glu53del)	rs878852993
NM_002468.5(MYD88):c.463+1G>A	rs2125777824

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