rs2228529, ERCC6

N. diseases: 4
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.
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19 0.020 1.000 2 2012 2017
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19 0.010 1.000 1 2012 2012
Experimental Organism Basal Cell Carcinoma
63 0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19 0.010 1.000 1 2012 2012
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19 0.010 1.000 1 2019 2019