Gene: NRXN1 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10490175
rs10490175
NRXN1
2 1.000 0.040 2 50855616 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs1045881
rs1045881
NRXN1
1 1.000 0.040 2 49921834 3 prime UTR variant C/T snv 0.15 0.010 < 0.001 1 2011 2011
dbSNP: rs10490162
rs10490162
NRXN1
1 1.000 0.040 2 51020519 intron variant T/C snv 0.14 0.010 1.000 1 2014 2014
dbSNP: rs10490168
rs10490168
NRXN1
1 1.000 0.040 2 50908336 intron variant C/T snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs112638127
rs112638127
NRXN1
1 1.000 0.040 2 50472460 missense variant T/C snv 4.0E-05 4.2E-05 0.010 < 0.001 1 2011 2011
dbSNP: rs12467557
rs12467557
NRXN1
1 1.000 0.040 2 51015132 intron variant A/G snv 9.2E-02 0.010 1.000 1 2014 2014
dbSNP: rs13382584
rs13382584
NRXN1
1 1.000 0.040 2 51020156 intron variant T/C snv 0.27 0.010 1.000 1 2011 2011
dbSNP: rs1558852
rs1558852
NRXN1
1 1.000 0.040 2 51024999 intron variant A/C;G snv 0.23 0.010 1.000 1 2011 2011
dbSNP: rs2024513
rs2024513
NRXN1
1 1.000 0.040 2 50924881 intron variant A/G snv 0.34 0.010 1.000 1 2011 2011