Source: UNIPROT

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: rs121913381
rs121913381
9 21971037 missense variant C/A;T snv
CUI: C0027533
Disease: Neck Neoplasms
Neck Neoplasms
0.700 0
dbSNP: rs747621669
rs747621669
9 21970988 missense variant C/T snv 4.1E-06
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 0
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 0
dbSNP: rs104894094
rs104894094
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs104894094
rs104894094
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06
CUI: C1838547
Disease: MELANOMA-PANCREATIC CANCER SYNDROME
MELANOMA-PANCREATIC CANCER SYNDROME
0.800 1.000 1 1994 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm
0.700 0
dbSNP: rs104894097
rs104894097
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.700 0
dbSNP: rs104894095
rs104894095
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs104894098
rs104894098
0.851 0.200 9 21970982 missense variant A/T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs104894099
rs104894099
0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs137854599
rs137854599
0.882 0.080 9 21971093 missense variant C/G;T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs749714198
rs749714198
0.882 0.200 9 21971100 missense variant G/A snv 8.6E-06 7.0E-06
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 1.000 12 1994 2009
dbSNP: rs758389471
rs758389471
0.882 0.080 9 21971160 missense variant C/G;T snv 4.7E-06; 4.7E-06
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 1.000 12 1994 2009
dbSNP: rs878853647
rs878853647
0.882 0.120 9 21971099 missense variant C/G;T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 1.000 12 1994 2009
dbSNP: rs1064794292
rs1064794292
0.882 0.200 9 21974760 missense variant C/T snv
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm
0.700 0
dbSNP: rs1064794292
rs1064794292
0.882 0.200 9 21974760 missense variant C/T snv
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 0 2009 2009
dbSNP: rs199907548
rs199907548
0.882 0.160 9 21974682 missense variant A/C;G snv 6.3E-04
CUI: C0005426
Disease: Biliary Tract Neoplasm
Biliary Tract Neoplasm
0.700 0
dbSNP: rs1554653960
rs1554653960
0.925 0.040 9 21971007 missense variant C/T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 1.000 12 1994 2009
dbSNP: rs876658534
rs876658534
0.925 0.120 9 21971156 missense variant GC/AA mnv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 1.000 12 1994 2009
dbSNP: rs878853650
rs878853650
0.925 0.120 9 21974733 missense variant A/G snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 1.000 12 1994 2009
dbSNP: rs113798404
rs113798404
0.925 0.080 9 21970995 missense variant C/G;T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.800 0
dbSNP: rs113798404
rs113798404
0.925 0.080 9 21970995 missense variant C/G;T snv
CUI: C0005426
Disease: Biliary Tract Neoplasm
Biliary Tract Neoplasm
0.700 0
dbSNP: rs372266620
rs372266620
0.925 0.120 9 21971189 missense variant G/A;C;T snv 9.1E-05; 2.3E-05; 9.1E-06
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.700 0
dbSNP: rs754806883
rs754806883
0.925 0.160 9 21971063 missense variant C/A;G;T snv 4.3E-06; 8.5E-06
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.700 0