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: rs9391701
rs9391701
MUC22
4 1.000 6 31015486 intron variant G/A snv 0.11 0.700 1.000 2 2009 2010
dbSNP: rs10039039
rs10039039
KCNIP1
5 1.000 5 170487960 intron variant C/T snv 8.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1005585
rs1005585
CBS
5 1.000 21 43056923 intron variant T/C snv 6.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs10173355
rs10173355
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A9
6 1.000 2 233688675 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10182825
rs10182825
PPP1CB ; SPDYA
5 1.000 2 28788221 intron variant G/A snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10467472
rs10467472
RGCC
5 1.000 13 41459562 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10495970
rs10495970 		5 1.000 2 49264671 intron variant G/A snv 0.26 0.700 1.000 1 2014 2014
dbSNP: rs10501678
rs10501678
GRM5
4 1.000 11 88708934 intron variant C/T snv 3.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs10509586
rs10509586
LINC01374
5 1.000 10 89981680 intron variant G/T snv 7.1E-02 0.700 1.000 1 2014 2014
dbSNP: rs10808739
rs10808739
CYP7B1
6 0.882 8 64727703 intron variant G/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs10947091
rs10947091
HCG20
4 1.000 6 30779439 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10947095
rs10947095
HCG20
4 1.000 6 30789798 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs11649112
rs11649112
SHISA9 ; LOC107984137
5 0.925 16 13267554 intron variant G/A snv 0.22 0.700 1.000 1 2015 2015
dbSNP: rs11758688
rs11758688
HCG20
4 1.000 6 30790571 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs11905359
rs11905359
TMEM230
5 1.000 20 5079306 intron variant C/A snv 7.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs12122100
rs12122100
NBPF13P ; LOC728989
4 1.000 1 147037378 intron variant T/C snv 0.76 0.800 1.000 1 2009 2009
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs12207756
rs12207756
CDSN ; PSORS1C1
4 1.000 6 31118905 intron variant C/T snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs12460243
rs12460243
FBN3
5 0.925 19 8066356 intron variant G/A snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs12526481
rs12526481
HCG20
4 1.000 6 30778856 intron variant C/A snv 0.33 0.700 1.000 1 2010 2010
dbSNP: rs12527415
rs12527415
HCG20
4 1.000 6 30786763 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs12532102
rs12532102
CDCA7L
5 1.000 7 21927090 intron variant A/G snv 0.82 0.700 1.000 1 2019 2019
dbSNP: rs12663103
rs12663103
GPSM3
7 0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs12697941
rs12697941
MUCL3 ; SFTA2
4 1.000 6 30936937 intron variant G/A snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs12722486
rs12722486
IL2RA
5 1.000 10 6061799 intron variant C/A;T snv 0.700 1.000 1 2014 2014