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: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.010 1.000 1 2007 2007
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2007 2007
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2009 2009
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2007 2007
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C1332153
Disease: acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome
acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome 		0.010 1.000 1 2007 2007
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2007 2007
dbSNP: rs1982151
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2009 2009