Source: CURATED ×
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: rs10261922
rs10261922 		1 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1037351
rs1037351
DDC ; FIGNL1
1 1.000 0.120 7 50497706 intron variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs10821936
rs10821936
ARID5B
2 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.810 1.000 4 2009 2019
dbSNP: rs10821938
rs10821938
ARID5B
1 0.925 0.120 10 61965014 intron variant A/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10899736
rs10899736
DDC ; FIGNL1
1 1.000 0.120 7 50479227 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10949482
rs10949482
NHLRC1
1 1.000 0.120 6 18121083 3 prime UTR variant C/T snv 6.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs10994982
rs10994982
ARID5B
1 0.790 0.120 10 61950345 intron variant A/G snv 0.49 0.710 1.000 2 2009 2019
dbSNP: rs11013046
rs11013046
PIP4K2A
1 1.000 0.120 10 22551654 intron variant C/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs1110701
rs1110701 		1 1.000 0.120 7 50410929 intergenic variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs11155133
rs11155133
LOC102723724
2 0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 0.800 1.000 1 2009 2009
dbSNP: rs112141546
rs112141546
ADAMTS18
1 1.000 0.120 16 77367618 missense variant C/A;G;T snv 4.0E-06; 1.4E-03 0.700 1.000 1 2016 2016
dbSNP: rs1135401746
rs1135401746
GNB1
7 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
dbSNP: rs1142345
rs1142345
TPMT
1 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs11575387
rs11575387
DDC ; FIGNL1
1 1.000 0.120 7 50499737 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs11575575
rs11575575
FIGNL1
1 1.000 0.120 7 50456510 intron variant C/A snv 7.5E-02 0.700 1.000 1 2013 2013
dbSNP: rs11770117
rs11770117 		2 1.000 0.120 7 50406065 downstream gene variant A/T snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs11978267
rs11978267
IKZF1
3 0.763 0.240 7 50398606 intron variant A/G snv 0.25 0.810 1.000 4 2009 2019
dbSNP: rs121909646
rs121909646
FLT3
3 0.882 0.120 13 28018504 missense variant T/A;G snv 0.700 0
dbSNP: rs121913232
rs121913232
FLT3
2 0.925 0.120 13 28018500 missense variant G/C snv 0.700 0
dbSNP: rs121913487
rs121913487
FLT3
2 0.925 0.120 13 28018503 missense variant A/C;T snv 0.700 0
dbSNP: rs121913488
rs121913488
FLT3
3 0.807 0.120 13 28018505 missense variant C/A;G;T snv 0.700 0
dbSNP: rs12540874
rs12540874
GRB10
2 0.882 0.280 7 50597225 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs12669559
rs12669559
IKZF1
3 1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 0.700 1.000 1 2013 2013
dbSNP: rs12719019
rs12719019 		2 1.000 0.120 7 50408441 downstream gene variant C/T snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs12719039
rs12719039
IKZF1
1 1.000 0.120 7 50351251 intron variant T/C snv 0.25 0.700 1.000 1 2013 2013