List of variants in gene NRXN1 studied for Intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001330078.2(NRXN1):c.322C>T (p.Pro108Ser)	rs199784029	0.00138
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser)	rs200792504	0.00074
NM_001330078.2(NRXN1):c.1158+26A>T	rs201802152	0.00069
NM_001330078.2(NRXN1):c.739C>G (p.Arg247Gly)	rs200009780	0.00001
NM_001330078.2(NRXN1):c.1697T>C (p.Leu566Pro)	rs1667698491
NM_001330078.2(NRXN1):c.2731A>G (p.Thr911Ala)	rs2091701971
NM_001330078.2(NRXN1):c.3112T>G (p.Ser1038Ala)	rs2089576800
NM_001330078.2(NRXN1):c.773-1G>T	rs1574949440
NM_001330078.2(NRXN1):c.832+42589_832+123997del

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