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: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0018498
Disease: Hair Color
Hair Color 		0.800 1.000 4 2008 2018
dbSNP: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0015396
Disease: Eye Color
Eye Color 		0.800 1.000 3 2010 2013
dbSNP: rs1667394
rs1667394
HERC2
15 28285036 intron variant C/A;T snv
CUI: C0015396
Disease: Eye Color
Eye Color 		0.800 1.000 3 2007 2018
dbSNP: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
dbSNP: rs1667394
rs1667394
HERC2
15 28285036 intron variant C/A;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.800 1.000 1 2007 2007
dbSNP: rs916977
rs916977
HERC2
1.000 0.080 15 28268218 intron variant T/C;G snv
CUI: C0015396
Disease: Eye Color
Eye Color 		0.800 1.000 1 2008 2013
dbSNP: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 3 2013 2018
dbSNP: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.700 1.000 2 2015 2018
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 2 2016 2019
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 2 2016 2019
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 2 2016 2019
dbSNP: rs1667392
rs1667392
HERC2
15 28288419 intron variant G/A;C;T snv
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.700 1.000 2 2015 2018
dbSNP: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal 		0.700 1.000 1 2018 2018
dbSNP: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.700 1.000 1 2018 2018
dbSNP: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.700 1.000 1 2018 2018
dbSNP: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs1129038
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.700 1.000 1 2018 2018
dbSNP: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2015 2015
dbSNP: rs12913832
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal 		0.700 1.000 1 2018 2018
dbSNP: rs12916300
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		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: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		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: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		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: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		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: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2017 2017