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: rs1042363
rs1042363
AKAP12
4 0.882 0.080 6 151356693 3 prime UTR variant T/C snv 0.020 1.000 2 2005 2006
dbSNP: rs1047383
rs1047383
PLCB1
1 20 8884359 3 prime UTR variant C/T snv 0.56 0.010 1.000 1 2017 2017
dbSNP: rs10784339
rs10784339
AVPR1A
1 12 63144866 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs17228602
rs17228602
ACHE ; UFSP1
2 7 100890786 3 prime UTR variant C/T snv 1.5E-02 0.010 1.000 1 2019 2019
dbSNP: rs17228616
rs17228616
ACHE ; UFSP1
3 1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs25531
rs25531
SLC6A4 ; LOC105371720
72 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 0.010 1.000 1 2014 2014