ClinVar Miner

List of variants in gene PCDH19 reported as likely benign for not provided

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Total variants: 11
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NM_001184880.2(PCDH19):c.1401G>T (p.Thr467=) rs794726896
NM_001184880.2(PCDH19):c.1602G>A (p.Leu534=)
NM_001184880.2(PCDH19):c.1612G>A (p.Gly538Ser)
NM_001184880.2(PCDH19):c.1618C>T (p.Leu540Phe) rs374593325
NM_001184880.2(PCDH19):c.3308A>G (p.Asn1103Ser)
NM_001184880.2(PCDH19):c.3319C>G (p.Arg1107Gly) rs191333060
NM_001184880.2(PCDH19):c.3439G>A (p.Val1147Ile) rs138771033
NM_001184880.2(PCDH19):c.769G>C (p.Val257Leu) rs201713027
NM_001184880.2(PCDH19):c.792T>C (p.Asp264=)

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