rs1048230, SLC11A2

N. diseases: 5
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2000 2000
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1 2000 2000
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2015 2015
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2000 2000