Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.100 0.909 11 2005 2013
dbSNP: rs3789243
rs3789243
0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.020 1.000 2 2009 2013
dbSNP: rs2032582
rs2032582
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 < 0.001 1 2007 2007
dbSNP: rs2229109
rs2229109
0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2008 2008
dbSNP: rs3842
rs3842
0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2009 2009