Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10255299
rs10255299
7 111887504 intron variant G/A snv 0.11
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2013 2013
dbSNP: rs10411936
rs10411936
1.000 0.080 19 16437564 intron variant A/G snv 0.63
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10489673
rs10489673
1 157580276 intron variant T/C;G snv 0.43; 8.0E-06
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10489844
rs10489844
1 158758599 intron variant C/T snv 0.25
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10494322
rs10494322
1 159367158 intron variant T/C snv 0.15
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs1057024
rs1057024
1 159020457 synonymous variant A/G snv 0.22 0.32
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs1065457
rs1065457
1 158354635 missense variant A/G snv 0.45 0.52
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10737176
rs10737176
1 160542826 3 prime UTR variant G/A snv 0.71
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10752631
rs10752631
1 159892363 intron variant T/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10752632
rs10752632
1 159905665 downstream gene variant G/A snv 0.54
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10796961
rs10796961
1 156586529 synonymous variant G/A snv 0.92 0.79
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10797007
rs10797007
1 158325839 downstream gene variant A/G snv 0.50
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908505
rs10908505
1 156498451 intron variant T/A;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908581
rs10908581
1 157668485 intergenic variant A/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908584
rs10908584
1 157671968 downstream gene variant T/A;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908702
rs10908702
1 159258588 intergenic variant C/T snv 0.46
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908709
rs10908709
1 159350390 intron variant C/A snv 0.34
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908710
rs10908710
1 159351189 non coding transcript exon variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908711
rs10908711
1 159351469 non coding transcript exon variant G/A snv 0.40
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908713
rs10908713
1 159369769 intron variant T/C snv 0.47
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10908714
rs10908714
1 159370563 intron variant T/A snv 0.38
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10917587
rs10917587
1 162691673 intron variant A/G snv 8.6E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10918137
rs10918137
1 161892765 intron variant G/A snv 0.49
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10918341
rs10918341
1 161980609 downstream gene variant A/G snv 0.51
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs10918342
rs10918342
1 161980661 downstream gene variant G/A snv 0.51
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011