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: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma 		0.900 0.952 6 2009 2020
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81
CUI: C0017638
Disease: Glioma
Glioma 		0.820 1.000 2 2009 2018
dbSNP: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.810 0.667 1 2011 2015
dbSNP: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.800 1.000 5 2009 2014
dbSNP: rs2297441
rs2297441
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
0.807 0.160 20 63696229 3 prime UTR variant G/A;C snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 1 2011 2011
dbSNP: rs4809324
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02
CUI: C0017638
Disease: Glioma
Glioma 		0.800 1.000 1 2009 2009
dbSNP: rs4809324
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.800 1.000 1 2009 2009
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.730 1.000 2 2010 2018
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		0.730 1.000 2 2010 2018
dbSNP: rs2236507
rs2236507
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.040 20 63691653 intron variant G/C;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.700 1.000 1 2015 2015
dbSNP: rs2236507
rs2236507
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.040 20 63691653 intron variant G/C;T snv
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 1 2015 2015
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 1 2017 2017
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs2738783
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs3208007
rs3208007
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs3208007
rs3208007
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2018 2018