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: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2017 2017
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2017 2017
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2017 2017
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1635168
rs1635168
HERC2
1.000 0.040 15 28290120 intron variant A/C snv 0.77
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
dbSNP: rs1667392
rs1667392
HERC2
15 28288419 intron variant G/A;C;T snv
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs1667394
rs1667394
HERC2
15 28285036 intron variant C/A;T snv
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs75165924
rs75165924
HERC2
15 28135112 intron variant C/T snv 7.0E-02
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs77572354
rs77572354
HERC2
15 28315576 intron variant C/G;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs79097182
rs79097182
HERC2
15 28266851 intron variant C/T snv 6.1E-02
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2015 2015
dbSNP: rs8033755
rs8033755
HERC2
1.000 0.080 15 28136400 intron variant C/A snv 0.84
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2016 2016