Gene: NRXN3 ×
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: rs7141420
rs7141420
NRXN3
5 1.000 0.080 14 79433111 intron variant C/T snv 0.56 0.700 1.000 6 2015 2019
dbSNP: rs10150332
rs10150332
NRXN3
4 14 79470621 intron variant T/C snv 0.26 0.700 1.000 2 2010 2019
dbSNP: rs7144011
rs7144011
NRXN3
4 1.000 0.080 14 79474040 intron variant G/T snv 0.21 0.700 1.000 2 2018 2019
dbSNP: rs17109256
rs17109256
NRXN3
3 14 79473650 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs2370982
rs2370982
NRXN3
1 14 79424334 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs72690737
rs72690737
NRXN3
1 14 79464301 intron variant T/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs8009329
rs8009329
NRXN3
1 14 79029342 intron variant A/G snv 0.56 0.700 1.000 1 2019 2019