Source: BEFREE

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: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma
0.710 1.000 1 2001 2001
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0025202
Disease: melanoma
melanoma
0.100 1.000 11 1997 2016
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 0.500 2 2002 2006
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2002 2003
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0027962
Disease: Melanocytic nevus
Melanocytic nevus
0.010 1.000 1 2002 2002
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0260037
Disease: Multiple tumors
Multiple tumors
0.010 1.000 1 2001 2001
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0030354
Disease: Papilloma
Papilloma
0.010 1.000 1 2002 2002
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2002 2002
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2008 2008
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0280100
Disease: Solid Neoplasm
Solid Neoplasm
0.010 1.000 1 2003 2003
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C4721414
Disease: Mantle cell lymphoma
Mantle cell lymphoma
0.010 1.000 1 2012 2012
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0039590
Disease: Testicular Neoplasms
Testicular Neoplasms
0.010 1.000 1 2003 2003
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2002 2002
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2004 2004
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C1257965
Disease: Compensatory Hyperinsulinemia
Compensatory Hyperinsulinemia
0.010 1.000 1 2008 2008
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2012 2012
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2006 2006
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0023418
Disease: leukemia
leukemia
0.010 1.000 1 2003 2003
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.010 1.000 1 2006 2006
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2008 2008
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2008 2008
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0004565
Disease: Melanoma, B16
Melanoma, B16
0.010 < 0.001 1 2006 2006