List of variants reported as pathogenic for perceptual disorders by Institute of Human Genetics, University of Goettingen

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000307.5(POU3F4):c.340dup (p.Trp114fs)	rs2147996471
NM_000390.4(CHM):c.232C>T (p.Gln78Ter)	rs2147706580
NM_000390.4(CHM):c.368_390dup (p.Thr131delinsLeuLeuTer)	rs2147676302
NM_001278431.2(C1QTNF5):c.562C>A (p.Pro188Thr)	rs1591299252
NM_001371596.2(MFSD8):c.698+2T>A
NM_144672.4(OTOA):c.938del (p.Ser313fs)
NM_177398.4(LMX1A):c.622C>T (p.Arg208Ter)	rs1396081975

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