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: rs1056629
rs1056629
MPHOSPH6
6 0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 0.010 1.000 1 2016 2016
dbSNP: rs1057519975
rs1057519975
TP53
34 0.649 0.480 17 7675209 missense variant A/C;G;T snv 0.010 1.000 1 2006 2006
dbSNP: rs121908585
rs121908585
PDGFRA
9 0.827 0.080 4 54285926 missense variant A/T snv 0.010 1.000 1 2019 2019
dbSNP: rs761887139
rs761887139
GLB1
2 0.925 0.160 3 33051997 missense variant G/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs8103851
rs8103851
PRKCG
5 0.851 0.040 19 53894400 intron variant C/G snv 0.44 0.010 1.000 1 2014 2014