Source: GWASDB

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: rs4785751
rs4785751
DEF8
1.000 0.040 16 89963009 intron variant G/A snv 0.37
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2011 2011
dbSNP: rs7195043
rs7195043
DEF8
1.000 0.040 16 89954453 intron variant C/T snv 0.58
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2011 2011
dbSNP: rs8051733
rs8051733
DEF8
1.000 0.040 16 89957798 intron variant A/G snv 0.30
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2011 2011