Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113488022
rs113488022
BRAF
490 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2013 2015
dbSNP: rs121913377
rs121913377
BRAF
480 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.020 1.000 2 2013 2015
dbSNP: rs1034749666
rs1034749666
OLIG2
9 0.776 0.160 21 33027257 missense variant G/A snv 0.010 1.000 1 2013 2013
dbSNP: rs121913500
rs121913500
IDH1
96 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs121913529
rs121913529
KRAS
144 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs199643834
rs199643834
MPRIP ; FLCN
6 0.827 0.200 17 17215000 missense variant T/C snv 1.9E-04 1.7E-04 0.010 1.000 1 2008 2008
dbSNP: rs762846821
rs762846821
TP53
57 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs764882391
rs764882391
MUC1
1 1.000 0.040 1 155187358 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 2013 2013
dbSNP: rs772667594
rs772667594
MUC1
1 1.000 0.040 1 155187332 missense variant T/C snv 8.0E-06 0.010 1.000 1 2013 2013