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: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
0.700 1.000 1 2016 2016
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 1997 1997
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2007 2007
dbSNP: rs104894104
rs104894104
0.790 0.160 9 21971019 missense variant G/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2007 2007