rs16891982, SLC45A2

N. diseases: 13
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hair Color
CUI: C0018498
Disease: Hair Color
312 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.800 1.000 3 2010 2018
Skin Pigmentation
CUI: C0037290
Disease: Skin Pigmentation
72 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.800 1.000 3 2007 2018
Eye Color
CUI: C0015396
Disease: Eye Color
31 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.800 1.000 2 2010 2018
melanoma
CUI: C0025202
Disease: melanoma
515 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.750 0.833 6 2008 2017
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.710 1.000 2 2009 2016
Suntan
CUI: C0406208
Disease: Suntan
94 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.700 1.000 2 2018 2018
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.700 1.000 1 2019 2019
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.700 1.000 1 2019 2019
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.700 1.000 1 2019 2019
Albinism, Oculocutaneous
CUI: C0078918
Disease: Albinism, Oculocutaneous
45 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.010 1.000 1 2015 2015
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.010 1.000 1 2009 2009
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.010 1.000 1 2009 2009
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
13 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.010 1.000 1 2010 2010