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: rs1145949
rs1145949
14 73239461 intron variant T/G snv 8.1E-03
RDW - Red blood cell distribution width result
0.700 1.000 1 2016 2016
dbSNP: rs1145949
rs1145949
14 73239461 intron variant T/G snv 8.1E-03
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs177389
rs177389
14 73260801 missense variant T/C;G snv 3.9E-02; 0.57
CUI: C0233849
Disease: Personality Traits
Personality Traits
Behavior and Behavior Mechanisms 0.700 1.000 1 2013 2013
dbSNP: rs1980413
rs1980413
14 73269615 intron variant G/C snv 0.19
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs61986932
rs61986932
14 73245245 splice acceptor variant C/A snv 5.6E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs61986932
rs61986932
14 73245245 splice acceptor variant C/A snv 5.6E-02
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019