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: 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: rs104894097
rs104894097
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05
CUI: C0025202
Disease: melanoma
melanoma
0.750 1.000 5 1995 2015
dbSNP: rs104894097
rs104894097
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 19 1995 2015
dbSNP: rs104894097
rs104894097
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma
0.700 1.000 16 1995 2015
dbSNP: rs104894097
rs104894097
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05
CUI: C1838547
Disease: MELANOMA-PANCREATIC CANCER SYNDROME
MELANOMA-PANCREATIC CANCER SYNDROME
0.700 1.000 13 1998 2016
dbSNP: rs104894097
rs104894097
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
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
CUI: C1835042
Disease: Melanoma astrocytoma syndrome
Melanoma astrocytoma syndrome
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
CUI: C0206754
Disease: Neuroendocrine Tumors
Neuroendocrine Tumors
0.010 1.000 1 2019 2019