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: rs11676922
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2010 2014
dbSNP: rs10209110
rs10209110
AFF3
1.000 0.120 2 100056230 intron variant C/T snv 0.47
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2012 2012
dbSNP: rs6712515
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2012 2012
dbSNP: rs4851221
rs4851221
AFF3
2 99663560 intron variant G/A snv 0.85
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs10496344
rs10496344
AFF3
2 100147663 intron variant T/C;G snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs11123810
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2016 2016
dbSNP: rs11123810
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs11123811
rs11123811
AFF3
1.000 0.120 2 100143710 intron variant T/C snv 0.55
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs11123816
rs11123816
AFF3
2 100167191 intron variant G/A snv 0.20
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs11676922
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs11676922
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs11676922
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs11677607
rs11677607
AFF3
2 100134688 intron variant C/T snv 0.24
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11692867
rs11692867
AFF3
2 100143015 intron variant G/A snv 0.34
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12712073
rs12712073
AFF3
2 100188666 intron variant T/C snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs13001130
rs13001130
AFF3
2 100052237 intron variant G/A snv 0.15
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs13002946
rs13002946
AFF3
2 100185497 intron variant T/A snv 0.25
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs13023088
rs13023088
AFF3
2 99959842 intron variant C/T snv 0.13
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs13032879
rs13032879
AFF3
2 99986297 intron variant C/T snv 0.13
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs13415465
rs13415465
AFF3
2 100147542 intron variant T/G snv 0.37
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs13415583
rs13415583
AFF3
1.000 0.120 2 100147625 intron variant T/G snv 0.37
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs144507626
rs144507626
AFF3
2 99825511 non coding transcript exon variant A/C snv 7.0E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17023314
rs17023314
AFF3
1.000 0.040 2 99931297 intron variant T/C snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17023459
rs17023459
AFF3
2 100067088 intron variant C/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17436893
rs17436893
AFF3
1.000 0.040 2 99924472 intron variant C/T snv 6.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017