Gene: NRGN ×
Source: GWASCAT ×
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