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: rs11599775
rs11599775
VTI1A
2 1.000 0.040 10 112699938 intron variant G/A snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs11706832
rs11706832
LRIG1
2 1.000 0.040 3 66452557 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs11979158
rs11979158
EGFR
5 0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs12021720
rs12021720
DBT
3 0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 0.700 1.000 1 2009 2009
dbSNP: rs12076373
rs12076373
AKT3
2 1.000 0.040 1 243688645 intron variant G/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs12088062
rs12088062 		2 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs12125049
rs12125049
LINC02778 ; LOC105378761
2 1.000 0.040 1 60202030 intergenic variant C/T snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs12230172
rs12230172
LOC105369844
4 0.882 0.040 12 75848895 intron variant A/G snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs12723208
rs12723208
TRAF5
2 1.000 0.040 1 211337552 intron variant A/G snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs12752552
rs12752552
RAVER2
4 0.882 0.040 1 64763616 intron variant T/C snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs1275600
rs1275600
LOC105369844
2 1.000 0.040 12 75869771 intron variant T/A snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs1409785
rs1409785 		2 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 0.700 1.000 1 2009 2009
dbSNP: rs16838813
rs16838813 		2 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs17110757
rs17110757
ACOT11
2 1.000 0.040 1 54584133 intron variant G/A snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs1801591
rs1801591
ETFA
4 0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs2235573
rs2235573
SLC16A8
4 0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 0.700 1.000 1 2017 2017
dbSNP: rs2236507
rs2236507
RTEL1 ; RTEL1-TNFRSF6B
2 1.000 0.040 20 63691653 intron variant G/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs2252586
rs2252586 		5 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs2297440
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
10 0.763 0.080 20 63680946 intron variant T/C snv 0.81 0.700 1.000 1 2017 2017
dbSNP: rs2562152
rs2562152
RHBDF1
4 0.882 0.040 16 73898 intron variant A/T snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs2853676
rs2853676
TERT
29 0.667 0.560 5 1288432 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs35850753
rs35850753
TP53
8 0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs3751667
rs3751667
LMF1
4 1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 0.700 1.000 1 2017 2017
dbSNP: rs3851634
rs3851634
POLR3B
4 0.882 0.040 12 106419124 intron variant T/C snv 0.22 0.700 1.000 1 2015 2015
dbSNP: rs4252707
rs4252707
MDM4
2 1.000 0.040 1 204539019 intron variant G/A snv 0.17 0.700 1.000 1 2017 2017