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: rs62331150
rs62331150
1.000 0.080 4 105147856 intron variant G/T snv 0.42
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs974801
rs974801
4 105149907 intron variant A/G snv 0.36
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs6533181
rs6533181
4 105153669 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2189234
rs2189234
1.000 0.040 4 105154341 intron variant T/G snv 0.62
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2015 2015
dbSNP: rs2189234
rs2189234
1.000 0.040 4 105154341 intron variant T/G snv 0.62
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs2189234
rs2189234
1.000 0.040 4 105154341 intron variant T/G snv 0.62
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs9790517
rs9790517
0.925 0.080 4 105163621 intron variant C/T snv 0.20
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.710 1.000 3 2013 2017
dbSNP: rs10022109
rs10022109
4 105166665 intron variant A/G snv 0.20
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs2903385
rs2903385
4 105173270 intron variant G/A snv 0.49
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2018 2018
dbSNP: rs2903385
rs2903385
4 105173270 intron variant G/A snv 0.49
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 2 2018 2019
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs139887111
rs139887111
4 105195057 intron variant -/T delins 0.31
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs1391440
rs1391440
4 105195804 intron variant C/G snv 0.50
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2019 2019
dbSNP: rs11726786
rs11726786
4 105199599 intron variant T/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 2 2017 2019
dbSNP: rs546941547
rs546941547
4 105204229 intron variant TATA/-;TA;TATATA delins 6.5E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
Malignant neoplasm of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019