Source: GWASCAT

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: rs7372960
rs7372960
1.000 0.040 3 71205600 intron variant T/C snv 0.21
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 3 2015 2019
dbSNP: rs11720523
rs11720523
3 71496019 intron variant C/A snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 2 2018 2018
dbSNP: rs17699658
rs17699658
3 71207158 intron variant C/T snv 0.17
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 2 2016 2019
dbSNP: rs17699658
rs17699658
3 71207158 intron variant C/T snv 0.17
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2016 2019
dbSNP: rs6779258
rs6779258
1.000 0.040 3 71500488 intron variant T/C snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 2 2019 2019
dbSNP: rs1653969
rs1653969
1.000 0.080 3 71282213 intron variant A/T snv 0.48
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2018 2018
dbSNP: rs17653411
rs17653411
1.000 0.040 3 71115027 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17699658
rs17699658
3 71207158 intron variant C/T snv 0.17
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs17718444
rs17718444
1.000 0.120 3 71450250 intron variant C/T snv 0.27
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps
0.700 1.000 1 2019 2019
dbSNP: rs1864896
rs1864896
3 71420694 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2116709
rs2116709
0.882 0.040 3 71572518 non coding transcript exon variant T/A snv 0.58
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs2116709
rs2116709
0.882 0.040 3 71572518 non coding transcript exon variant T/A snv 0.58
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs2116709
rs2116709
0.882 0.040 3 71572518 non coding transcript exon variant T/A snv 0.58
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
0.700 1.000 1 2016 2016
dbSNP: rs2321503
rs2321503
3 71157824 intron variant T/C snv 0.14
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2593855
rs2593855
3 71126344 intron variant C/T snv 0.30
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2017 2017
dbSNP: rs34346645
rs34346645
1.000 0.040 3 71508794 intron variant C/A snv 0.32
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2016 2016
dbSNP: rs35480566
rs35480566
3 71534026 intron variant A/G snv 0.33
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs35480566
rs35480566
3 71534026 intron variant A/G snv 0.33
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs35540156
rs35540156
0.882 0.040 3 71473027 intron variant A/G snv 0.42
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
0.700 1.000 1 2019 2019
dbSNP: rs35540156
rs35540156
0.882 0.040 3 71473027 intron variant A/G snv 0.42
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm
0.700 1.000 1 2019 2019
dbSNP: rs35540156
rs35540156
0.882 0.040 3 71473027 intron variant A/G snv 0.42
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs35592432
rs35592432
3 71306089 intron variant G/C snv 2.0E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs35956082
rs35956082
0.776 0.160 3 71414748 intron variant A/C;G snv
CUI: C0399352
Disease: Developmental absence of tooth
Developmental absence of tooth
0.700 1.000 1 2018 2018
dbSNP: rs35956082
rs35956082
0.776 0.160 3 71414748 intron variant A/C;G snv
CUI: C3489529
Disease: Tooth Agenesis, Familial
Tooth Agenesis, Familial
0.700 1.000 1 2018 2018
dbSNP: rs35956082
rs35956082
0.776 0.160 3 71414748 intron variant A/C;G snv
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
TOOTH AGENESIS, SELECTIVE, 9
0.700 1.000 1 2018 2018