Gene: NRGN ×
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: rs55661361
rs55661361
NRGN
3 1.000 0.040 11 124744061 intron variant G/A snv 0.43 0.700 1.000 8 2014 2019
dbSNP: rs12293670
rs12293670
NRGN
1 1.000 0.040 11 124743036 intron variant A/G snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs12278912
rs12278912
NRGN
3 0.882 0.040 11 124742263 intron variant G/A snv 0.33 0.030 1.000 3 2012 2016
dbSNP: rs7113041
rs7113041
NRGN
1 1.000 0.040 11 124742695 intron variant C/G snv 0.35 0.020 1.000 2 2008 2016