Source: CLINVAR

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: rs104894340
rs104894340
0.827 0.200 12 57751647 missense variant C/A;T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3
0.800 1.000 0 1995 1998
dbSNP: rs104894340
rs104894340
0.827 0.200 12 57751647 missense variant C/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.740 0.600 1 2003 2014
dbSNP: rs104894340
rs104894340
0.827 0.200 12 57751647 missense variant C/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs104894340
rs104894340
0.827 0.200 12 57751647 missense variant C/A;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs104894340
rs104894340
0.827 0.200 12 57751647 missense variant C/A;T snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.700 1.000 1 2016 2016