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: rs10249276
rs10249276 		1 7 118938630 intergenic variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10281955
rs10281955 		1 7 118944637 intergenic variant G/A snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs10433415
rs10433415 		1 3 133566686 intergenic variant G/T snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs10935068
rs10935068 		1 3 133543963 upstream gene variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10935070
rs10935070
TOPBP1
1 3 133623144 missense variant T/C;G snv 0.29; 4.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs10935073
rs10935073
TF ; INHCAP
1 3 133720340 intron variant T/C snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs10953881
rs10953881 		1 7 118968071 intergenic variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10953885
rs10953885 		1 7 118968349 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1107413
rs1107413
SRPRB ; LOC105374116
1 3 133805873 missense variant G/C snv 0.22 0.20 0.700 1.000 1 2011 2011
dbSNP: rs11128951
rs11128951 		1 3 20334054 intron variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs11208264
rs11208264
PGM1
1 1 63659401 intron variant T/C snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs115714636
rs115714636
ITIH3
1 3 52796511 missense variant A/G snv 1.6E-03 6.4E-03 0.700 1.000 1 2013 2013
dbSNP: rs11576729
rs11576729
PGM1
1 1 63648758 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs115888294
rs115888294 		1 8 94105161 upstream gene variant T/C snv 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs11766519
rs11766519 		1 7 57524150 intergenic variant T/C snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs11921187
rs11921187
RAB6B
1 3 133832798 intron variant T/C snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs11921527
rs11921527
TF ; INHCAP
1 3 133722323 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11993089
rs11993089
MSRA
1 8 10152442 intron variant G/T snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs12027168
rs12027168
PGM1
1 1 63654942 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12108602
rs12108602 		1 4 114719413 upstream gene variant A/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs12292796
rs12292796 		1 11 39404549 intergenic variant A/C snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs12639304
rs12639304
TF ; INHCAP
1 3 133722750 intron variant A/T snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs13250871
rs13250871 		1 8 11610254 intergenic variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs1358024
rs1358024
TF
1 3 133765344 intron variant C/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs1371187
rs1371187 		1 2 164188591 intron variant A/G snv 0.52 0.700 1.000 1 2018 2018