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: rs1558375
rs1558375
ABCB4
1 1.000 0.080 7 87449753 intron variant T/C snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs17209837
rs17209837 		1 1.000 0.080 7 87495506 intergenic variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs7504990
rs7504990
DCC
4 0.851 0.120 18 52991406 intron variant T/C snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs975334
rs975334
CNTN4
2 0.925 0.080 3 2804632 intron variant G/A snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs117856857
rs117856857
MYC ; CASC11
1 1.000 0.080 8 127736248 missense variant C/G snv 1.7E-02 0.010 1.000 1 2015 2015
dbSNP: rs28934571
rs28934571
TP53
31 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2017 2017