CNTN2, contactin 2, 6900

N. diseases: 99; N. variants: 14
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: rs3767297
rs3767297
1 205067698 non coding transcript exon variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs3820337
rs3820337
1 205045802 intron variant T/C;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs6593920
rs6593920
1 205068548 non coding transcript exon variant T/G snv 0.41
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018