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: rs2189234
rs2189234
TET2
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
TET2
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
TET2
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: rs2454205
rs2454205
TET2 ; TET2-AS1
4 105263072 intron variant C/T snv 0.43
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2454206
rs2454206
TET2 ; TET2-AS1
0.851 0.160 4 105275794 missense variant A/G;T snv 0.30; 6.4E-06
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2015 2015
dbSNP: rs2647257
rs2647257
TET2 ; TET2-AS1
4 105278348 3 prime UTR variant A/T snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs2726492
rs2726492
TET2 ; TET2-AS1
1.000 0.080 4 105274384 intron variant T/C snv 0.82
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs2726518
rs2726518
TET2 ; TET2-AS1
1.000 0.080 4 105252042 intron variant A/C snv 0.63
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs2903385
rs2903385
TET2 ; TET2-AS1
4 105173270 intron variant G/A snv 0.49
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2903385
rs2903385
TET2 ; TET2-AS1
4 105173270 intron variant G/A snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs546941547
rs546941547
TET2 ; TET2-AS1
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: rs56185013
rs56185013
TET2 ; TET2-AS1
4 105238976 3 prime UTR variant G/A snv 0.18
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs62331150
rs62331150
TET2
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: rs6533181
rs6533181
TET2
4 105153669 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6533183
rs6533183
TET2 ; TET2-AS1
4 105212027 intron variant C/T snv 0.61
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs6533183
rs6533183
TET2 ; TET2-AS1
4 105212027 intron variant C/T snv 0.61
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs6533183
rs6533183
TET2 ; TET2-AS1
4 105212027 intron variant C/T snv 0.61
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs6839705
rs6839705
TET2 ; TET2-AS1
4 105223578 intron variant A/C snv 0.61
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs6855629
rs6855629
TET2 ; TET2-AS1
4 105213159 intron variant G/A;T snv 0.28
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs7674220
rs7674220
TET2 ; TET2-AS1
1.000 0.040 4 105227601 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs7674220
rs7674220
TET2 ; TET2-AS1
1.000 0.040 4 105227601 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs7683416
rs7683416
TET2 ; TET2-AS1
4 105231827 intron variant T/C snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7683416
rs7683416
TET2 ; TET2-AS1
4 105231827 intron variant T/C snv 0.45
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs974801
rs974801
TET2
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