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: rs12386756
rs12386756
STEAP4
1 1.000 0.040 7 88301614 intron variant G/A;C;T snv 0.020 1.000 2 2010 2015
dbSNP: rs10033652
rs10033652
RASGEF1B
1 1.000 0.040 4 81571913 intron variant C/T snv 0.62 0.010 1.000 1 2019 2019
dbSNP: rs10085637
rs10085637
PDK4 ; LOC107986824
1 1.000 0.040 7 95596501 5 prime UTR variant T/C;G snv 0.40 0.010 1.000 1 2012 2012
dbSNP: rs10185316
rs10185316
INSIG2 ; LOC107985940
1 1.000 0.040 2 118086902 upstream gene variant C/G snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs1053239
rs1053239
CIDEC
1 1.000 0.040 3 9867065 3 prime UTR variant G/C snv 0.19; 5.6E-05 0.14 0.010 1.000 1 2017 2017
dbSNP: rs1055419
rs1055419
OSBPL11
1 1.000 0.040 3 125594988 5 prime UTR variant G/A snv 7.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs10746473
rs10746473
PER3
1 1.000 0.040 1 7817996 intron variant A/G snv 0.58 0.010 1.000 1 2017 2017
dbSNP: rs10749127
rs10749127
TCF7L2
1 1.000 0.040 10 113089594 intron variant C/T snv 0.28 0.010 1.000 1 2009 2009
dbSNP: rs10830956
rs10830956 		1 1.000 0.040 11 92947847 intergenic variant C/T snv 0.33 0.800 1.000 1 2011 2011
dbSNP: rs10845640
rs10845640
APOBEC1
1 1.000 0.040 12 7659861 intron variant C/T snv 0.34 0.010 1.000 1 2019 2019
dbSNP: rs10892044
rs10892044
SIK3
1 1.000 0.040 11 116896183 intron variant T/C snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs10920533
rs10920533
ADIPOR1
1 1.000 0.040 1 202956690 intron variant G/A snv 0.22 0.010 1.000 1 2010 2010
dbSNP: rs11066194
rs11066194
HECTD4
1 1.000 0.040 12 112212323 intron variant A/G snv 4.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs11082639
rs11082639
SMAD2
1 1.000 0.040 18 47900264 intron variant C/T snv 0.54 0.010 1.000 1 2017 2017
dbSNP: rs11123469
rs11123469
INSIG2 ; LOC107985940
1 1.000 0.040 2 118086607 upstream gene variant T/C snv 0.14 0.010 1.000 1 2012 2012
dbSNP: rs11187033
rs11187033
IDE
1 1.000 0.040 10 92502602 intron variant T/A snv 0.28 0.010 1.000 1 2009 2009
dbSNP: rs11216186
rs11216186
SIK3
1 1.000 0.040 11 116913976 intron variant T/C snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs1127065
rs1127065
CAMK2B
1 1.000 0.040 7 44220272 synonymous variant C/G;T snv 1.7E-02; 0.41 0.800 1.000 1 2012 2012
dbSNP: rs1133607
rs1133607
ACSM2A
1 1.000 0.040 16 20483086 missense variant C/G;T snv 4.0E-06; 0.13 0.010 1.000 1 2006 2006
dbSNP: rs115336700
rs115336700
SHBG
1 1.000 0.040 17 7631341 missense variant G/A;C snv 2.8E-05; 1.7E-03 0.010 1.000 1 2006 2006
dbSNP: rs11631342
rs11631342
LIPC ; ALDH1A2
1 1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs11654081
rs11654081
RAI1
1 1.000 0.040 17 17804815 intron variant T/C snv 0.51 0.010 1.000 1 2016 2016
dbSNP: rs11760281
rs11760281
CD36 ; GNAT3
1 1.000 0.040 7 80475233 intron variant A/G snv 0.55 0.010 1.000 1 2012 2012
dbSNP: rs11827828
rs11827828
SIK3
1 1.000 0.040 11 116884868 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs1184436054
rs1184436054
GNB3
1 1.000 0.040 12 6843683 missense variant C/T snv 7.0E-06 0.010 1.000 1 2011 2011