Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10411936
rs10411936
1.000 0.080 19 16437564 intron variant A/G snv 0.63
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs10404046
rs10404046
19 16366444 intron variant G/C snv 0.63
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs10408945
rs10408945
19 16466180 intron variant G/T snv 0.14
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs10411936
rs10411936
1.000 0.080 19 16437564 intron variant A/G snv 0.63
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2011 2011
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: rs1870071
rs1870071
1.000 0.080 19 16394295 intron variant T/C snv 0.37
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2290669
rs2290669
19 16384963 intron variant A/C;G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs3786586
rs3786586
19 16384476 intron variant A/G snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs7251806
rs7251806
19 16388758 intron variant C/A;G;T snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs78663649
rs78663649
19 16378636 intron variant C/T snv 8.0E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016