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: rs770692189
rs770692189
2 1.000 0.120 2 111123957 missense variant G/A;T snv 1.6E-05; 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs121918453
rs121918453
19 0.732 0.280 12 112450394 missense variant G/A;C;T snv 0.010 1.000 1 2007 2007
dbSNP: rs121918454
rs121918454
17 0.742 0.280 12 112450395 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs121918464
rs121918464
25 0.708 0.440 12 112450406 missense variant G/A;C snv 0.010 1.000 1 2007 2007
dbSNP: rs397507514
rs397507514
10 0.790 0.240 12 112450408 missense variant G/C;T snv 0.010 1.000 1 2007 2007
dbSNP: rs121434596
rs121434596
26 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs11536889
rs11536889
27 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 0.010 1.000 1 2017 2017
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2019 2019
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.020 1.000 2 2016 2019
dbSNP: rs724159947
rs724159947
6 0.851 0.120 12 11869601 missense variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs724159946
rs724159946
3 1.000 12 11884541 missense variant G/A snv 7.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs724159945
rs724159945
3 1.000 12 11885968 missense variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs267606706
rs267606706
CBL
9 0.807 0.240 11 119278181 missense variant T/A;C snv 8.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs757874631
rs757874631
CBL
4 0.882 0.120 11 119278211 missense variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs387906664
rs387906664
CBL
2 1.000 11 119278220 missense variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs757333753
rs757333753
6 0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs78245253
rs78245253
2 1.000 3 128485850 missense variant G/A;C snv 4.0E-06; 5.0E-03 0.010 1.000 1 2009 2009
dbSNP: rs2285489
rs2285489
2 9 133424254 intron variant T/C snv 0.68 0.010 1.000 1 2019 2019
dbSNP: rs1801271
rs1801271
2 5 150054082 missense variant T/A;C snv 0.700 1.000 1 1990 1990
dbSNP: rs121913393
rs121913393
2 5 150054083 missense variant A/G snv 0.700 1.000 1 1990 1990
dbSNP: rs1057519802
rs1057519802
2 5 150061765 missense variant A/C snv 0.700 1.000 1 2009 2009
dbSNP: rs1057520014
rs1057520014
1 5 150073480 missense variant C/A snv 0.700 1.000 1 1990 1990
dbSNP: rs121913390
rs121913390
2 5 150073481 stop gained A/G;T snv 0.700 1.000 1 1990 1990
dbSNP: rs7656411
rs7656411
8 0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 0.010 1.000 1 2017 2017
dbSNP: rs8192284
rs8192284
19 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2013 2013