Source: ALL

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: rs1061535
rs1061535
6 29970147 upstream gene variant T/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs115559990
rs115559990
6 29926633 non coding transcript exon variant C/G;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs1632879
rs1632879
6 29949926 downstream gene variant G/A snv 0.82
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1632883
rs1632883
6 29948216 downstream gene variant C/A snv 0.78
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1655904
rs1655904
6 29949369 downstream gene variant T/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs16896742
rs16896742
6 29954963 upstream gene variant A/G snv 0.35
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2014 2014
dbSNP: rs17882753
rs17882753
6 29944817 non coding transcript exon variant C/T snv 1.4E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs192543598
rs192543598
6 29963568 downstream gene variant A/G snv 1.6E-02
CUI: C2004491
Disease: Cicatrix
Cicatrix
0.700 1.000 1 2019 2019
dbSNP: rs192543598
rs192543598
6 29963568 downstream gene variant A/G snv 1.6E-02
Severe cutaneous adverse reactions (SMQ)
0.700 1.000 1 2019 2019
dbSNP: rs2499
rs2499
6 29945765 3 prime UTR variant T/G snv 0.87
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2508037
rs2508037
6 29950659 downstream gene variant T/C;G snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2012 2012
dbSNP: rs2523933
rs2523933
6 29964515 intergenic variant G/C;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs2571381
rs2571381
6 29945053 splice region variant T/A;C snv 0.85
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2571400
rs2571400
6 29959945 downstream gene variant C/G snv 0.51
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs28749114
rs28749114
6 29937675 upstream gene variant A/G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2975009
rs2975009
6 29930339 upstream gene variant C/T snv 0.50
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs3094141
rs3094141
6 29942030 5 prime UTR variant T/G snv 0.87
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs3893463
rs3893463
6 29967628 downstream gene variant C/T snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs5025708
rs5025708
6 29987422 intergenic variant G/T snv 0.92
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs6914699
rs6914699
6 29966245 downstream gene variant T/C snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs7739434
rs7739434
6 29962842 downstream gene variant G/A snv 0.78
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs9259819
rs9259819
6 29925798 upstream gene variant G/T snv 0.49
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs9260313
rs9260313
6 29949108 downstream gene variant T/C snv 0.42
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs9260313
rs9260313
6 29949108 downstream gene variant T/C snv 0.42
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs9260620
rs9260620
6 29955314 upstream gene variant T/G snv 0.24
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016