rs16891982, SLC45A2

N. diseases: 6
Source: BEFREE ×
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.
melanoma
CUI: C0025202
Disease: melanoma
352 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.750 0.833 5 2008 2017
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
197 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.710 1.000 1 2009 2016
Albinism, Oculocutaneous
CUI: C0078918
Disease: Albinism, Oculocutaneous
37 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
65 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