Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10754833
rs10754833
0.851 0.040 1 236021631 intron variant T/A;C snv
CUI: C0027962
Disease: Melanocytic nevus
Melanocytic nevus
0.010 1.000 1 2011 2011
dbSNP: rs10754833
rs10754833
0.851 0.040 1 236021631 intron variant T/A;C snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2011 2011
dbSNP: rs10754833
rs10754833
0.851 0.040 1 236021631 intron variant T/A;C snv
CUI: C0027960
Disease: Nevus
Nevus
0.010 1.000 1 2011 2011
dbSNP: rs10754833
rs10754833
0.851 0.040 1 236021631 intron variant T/A;C snv
CUI: C1456781
Disease: Benign melanocytic nevus
Benign melanocytic nevus
0.010 1.000 1 2011 2011