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: rs11158559
rs11158559
SPTB
2 14 64774231 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1320561
rs1320561 		2 20 23117243 intergenic variant G/A snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs169082
rs169082
DOCK2
1 5 169647052 intron variant C/T snv 0.45 0.700 1.000 1 2008 2008
dbSNP: rs6071166
rs6071166 		1 20 38704369 intergenic variant C/A snv 0.59 0.700 1.000 1 2016 2016
dbSNP: rs6738627
rs6738627
COBLL1 ; SNORA70F
2 2 164687940 intron variant G/A snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs7822058
rs7822058
LOC105375835
2 8 52772301 intergenic variant T/C snv 0.89 0.700 1.000 1 2012 2012
dbSNP: rs8043757
rs8043757
FTO
5 0.925 0.120 16 53779538 intron variant A/T snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs900400
rs900400
LINC02029
7 0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 0.700 1.000 1 2016 2016