ClinVar Miner

List of variants in gene NRXN1 studied for Pitt-Hopkins-like syndrome 2; Schizophrenia 17

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Total variants: 19
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HGVS dbSNP
NM_001135659.2(NRXN1):c.1820T>G (p.Leu607Trp) rs372311299
NM_001135659.2(NRXN1):c.1904G>A (p.Arg635His) rs761279630
NM_001135659.2(NRXN1):c.2098G>A (p.Ala700Thr) rs199939303
NM_001135659.2(NRXN1):c.2310G>T (p.Gln770His) rs199978276
NM_001135659.2(NRXN1):c.2579G>A (p.Ser860Asn) rs80293130
NM_001135659.2(NRXN1):c.262C>G (p.Arg88Gly) rs748684256
NM_001135659.2(NRXN1):c.2653C>T (p.His885Tyr) rs199784139
NM_001135659.2(NRXN1):c.270G>T (p.Gln90His) rs199960045
NM_001135659.2(NRXN1):c.2725C>A (p.Leu909Met) rs201818223
NM_001135659.2(NRXN1):c.302C>G (p.Ala101Gly) rs200184823
NM_001135659.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001135659.2(NRXN1):c.3485-109902C>T
NM_001135659.2(NRXN1):c.3485-109939C>T rs766942777
NM_001135659.2(NRXN1):c.3527C>T (p.Thr1176Met)
NM_001135659.2(NRXN1):c.3662A>G (p.His1221Arg) rs200915287
NM_001135659.2(NRXN1):c.4131G>C (p.Glu1377Asp) rs200935246
NM_001135659.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001135659.2(NRXN1):c.600C>T (p.Gly200=) rs201481698
NM_001135659.2(NRXN1):c.665_673dup (p.Glu224_Gly225insGluGlyGlu) rs774230140

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