rs121913371, BRAF

N. diseases: 3
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.
melanoma
CUI: C0025202
Disease: melanoma
515 1.000 0.040 7 140781678 missense variant G/A;T snv 4.0E-06; 8.0E-06 0.700 1.000 2 2007 2014
Constipation
CUI: C0009806
Disease: Constipation
57 1.000 0.040 7 140781678 missense variant G/A;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2004 2004
Hematochezia
CUI: C0018932
Disease: Hematochezia
12 1.000 0.040 7 140781678 missense variant G/A;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2004 2004