SNX7, sorting nexin 7, 51375

N. diseases: 9; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10783100
rs10783100
1 98710740 intron variant T/G snv 0.51
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs56242843
rs56242843
1 98723043 intron variant C/T snv 0.27
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018