Source: ALL
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: rs1057519823
rs1057519823
15 66481830 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 2 2009 2013
dbSNP: rs730880502
rs730880502
15 66436762 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 2 2009 2013
dbSNP: rs1057519730
rs1057519730
1.000 0.040 15 66436786 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1057519819
rs1057519819
0.851 0.240 15 66436750 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1057519820
rs1057519820
15 66436810 missense variant A/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1057519821
rs1057519821
15 66436814 missense variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1057519822
rs1057519822
0.925 0.080 15 66481818 missense variant T/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs1489477346
rs1489477346
15 66387359 synonymous variant G/A snv 5.8E-06 2.1E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2012 2012