Source: BEFREE ×
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: rs16139
rs16139
36 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 0.050 1.000 5 2006 2015
dbSNP: rs16147
rs16147
18 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 0.040 1.000 4 2012 2015
dbSNP: rs17149106
rs17149106
2 0.925 0.160 7 24283588 upstream gene variant G/T snv 0.020 1.000 2 2011 2016
dbSNP: rs16131
rs16131
1 1.000 0.080 7 24290218 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs16475
rs16475
2 0.925 0.120 7 24291867 downstream gene variant A/G snv 5.3E-02 0.010 1.000 1 2013 2013
dbSNP: rs5574
rs5574
5 0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 0.010 1.000 1 2015 2015