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: rs10485400
rs10485400
L3MBTL3 ; LOC105378000
1 1.000 0.080 6 130122979 intron variant C/T snv 0.43 0.010 1.000 1 2013 2013
dbSNP: rs10490072
rs10490072 		2 1.000 0.080 2 60442796 upstream gene variant T/C snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs10497511
rs10497511
NFE2L2
1 1.000 0.080 2 177254568 intron variant G/A;C snv 0.010 < 0.001 1 2016 2016
dbSNP: rs10498210
rs10498210
IRS1
1 1.000 0.080 2 226755230 intron variant G/A snv 9.0E-02 0.010 1.000 1 2019 2019
dbSNP: rs10507486
rs10507486
FOXO1
1 1.000 0.080 13 40612364 intron variant G/A snv 0.17 0.010 1.000 1 2009 2009
dbSNP: rs10507875
rs10507875
EDNRB ; OBI1-AS1
3 0.925 0.160 13 77943119 intron variant A/G snv 0.17 0.010 1.000 1 2018 2018
dbSNP: rs10509291
rs10509291 		6 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs1051295
rs1051295
KCNB1 ; LOC105372649
3 0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs10515353
rs10515353 		1 1.000 0.080 5 104585969 intron variant T/C snv 0.14 0.010 1.000 1 2007 2007
dbSNP: rs10517030
rs10517030
PPARGC1A
2 0.925 0.120 4 23961283 intergenic variant A/C snv 6.9E-02 0.010 1.000 1 2017 2017
dbSNP: rs10517032
rs10517032
PPARGC1A
2 0.925 0.120 4 23966759 regulatory region variant C/A snv 5.4E-02 0.010 1.000 1 2017 2017
dbSNP: rs10521253
rs10521253
COX10
1 1.000 0.080 17 14074847 intron variant A/G snv 6.9E-02 0.010 1.000 1 2012 2012
dbSNP: rs10524523
rs10524523
TOMM40
7 0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 0.010 1.000 1 2014 2014
dbSNP: rs1052717
rs1052717
SREBF2
3 0.925 0.080 22 41885425 intron variant A/G snv 0.62 0.010 < 0.001 1 2018 2018
dbSNP: rs1053049
rs1053049
PPARD
1 1.000 0.080 6 35427841 3 prime UTR variant C/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs1056285
rs1056285
MRS2
1 1.000 0.080 6 24420316 intron variant G/A;T snv 8.7E-02 0.010 1.000 1 2015 2015
dbSNP: rs1057520504
rs1057520504
HNF1A
4 0.882 0.080 12 120994238 missense variant G/A snv 0.010 < 0.001 1 2015 2015
dbSNP: rs1057910
rs1057910
CYP2C9
12 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1058046
rs1058046
PYY
2 0.925 0.120 17 43953163 missense variant G/C snv 0.63 0.59 0.010 1.000 1 2005 2005
dbSNP: rs1058405
rs1058405
ATF6
1 1.000 0.080 1 161781951 missense variant A/G;T snv 0.23; 8.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs1060499866
rs1060499866
HNF1A
2 0.925 0.080 12 120993532 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2009 2009
dbSNP: rs1062827
rs1062827
F11R
1 1.000 0.080 1 160997054 3 prime UTR variant C/T snv 0.22 0.010 1.000 1 2012 2012
dbSNP: rs1063537
rs1063537
ADIPOQ ; ADIPOQ-AS1
6 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs1063538
rs1063538
ADIPOQ ; ADIPOQ-AS1
4 1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55 0.010 1.000 1 2012 2012