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: rs9967983
rs9967983
SOD1
2 0.925 0.080 21 31665169 intron variant A/T snv 0.47 0.010 1.000 1 2013 2013
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2010 2010
dbSNP: rs9915936
rs9915936
AXIN2
5 0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 0.010 < 0.001 1 2011 2011
dbSNP: rs9900242
rs9900242
CASC17
2 0.925 0.080 17 71139490 intron variant G/A snv 0.32 0.010 1.000 1 2015 2015
dbSNP: rs9852810
rs9852810
MLH1
3 0.882 0.080 3 37027478 intron variant G/A snv 0.35 0.010 1.000 1 2010 2010
dbSNP: rs9832989
rs9832989
SLCO2A1
1 1.000 0.080 3 133982979 intron variant A/G snv 1.4E-02 0.700 1.000 1 2020 2020
dbSNP: rs980171
rs980171
PCAT1 ; LOC105375751
2 0.925 0.080 8 127042277 intron variant A/G snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs976306779
rs976306779
AR
8 0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 0.020 1.000 2 2005 2008
dbSNP: rs968098233
rs968098233
AR
3 0.882 0.200 X 67546162 missense variant T/C snv 0.010 1.000 1 2005 2005
dbSNP: rs9666607
rs9666607
CD44
2 0.925 0.080 11 35204608 missense variant A/G;T snv 0.74 0.010 1.000 1 2018 2018
dbSNP: rs9658655
rs9658655
CHGA
2 0.925 0.080 14 92931686 missense variant G/C snv 0.13 0.12 0.010 1.000 1 2010 2010
dbSNP: rs9651118
rs9651118
MTHFR
20 0.683 0.480 1 11802157 intron variant T/C snv 0.18 0.010 1.000 1 2016 2016
dbSNP: rs9644474
rs9644474
LINC02055
1 1.000 0.080 8 136150901 intron variant C/T snv 0.71 0.700 1.000 1 2020 2020
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.010 1.000 1 2014 2014
dbSNP: rs9625483
rs9625483
TTC28
1 1.000 0.080 22 28492951 intron variant G/A snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs9623117
rs9623117
TNRC6B
4 0.851 0.200 22 40056115 intron variant T/C snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs9608380
rs9608380
CRYBB2
2 0.925 0.080 22 25226475 intron variant C/T snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs9600079
rs9600079 		5 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 0.710 1.000 4 2010 2019
dbSNP: rs953038635
rs953038635
SOD2
51 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 0.020 1.000 2 2007 2009
dbSNP: rs946993012
rs946993012
NOS1
2 0.925 0.080 12 117331056 missense variant A/G snv 4.0E-06 1.4E-05 0.010 1.000 1 2009 2009
dbSNP: rs9469899
rs9469899
UHRF1BP1
1 1.000 0.080 6 34825347 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs9443189
rs9443189
MYO6
1 1.000 0.080 6 75786165 intron variant A/G snv 0.26 0.700 1.000 1 2014 2014
dbSNP: rs9393682
rs9393682
H1-2
2 0.925 0.080 6 26056822 upstream gene variant C/T snv 9.8E-02 0.010 1.000 1 2017 2017
dbSNP: rs9388766
rs9388766
L3MBTL3
3 0.925 0.080 6 130033710 intron variant T/C snv 0.65 0.010 1.000 1 2017 2017
dbSNP: rs9375701
rs9375701
L3MBTL3
6 0.827 0.160 6 130062912 intron variant C/T snv 0.53 0.010 1.000 1 2016 2016