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: rs1801591
rs1801591
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.710 1.000 2 2015 2017
dbSNP: rs77633900
rs77633900
1.000 0.040 15 76246118 intron variant G/C snv 6.3E-02
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.700 1.000 1 2017 2017