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: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2011 2017
dbSNP: rs11076008
rs11076008
FTO
2 0.925 0.120 16 53893411 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs16924573
rs16924573
KIAA1217
1 1.000 0.040 10 24315964 intron variant G/A snv 8.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs1793937
rs1793937
COL2A1 ; LOC105369752
1 1.000 0.040 12 47981692 intron variant C/G snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs1799750
rs1799750
MMP1 ; WTAPP1
48 0.592 0.760 11 102799765 intron variant C/- delins 0.50 0.010 1.000 1 2013 2013
dbSNP: rs1800012
rs1800012
COL1A1
13 0.763 0.320 17 50200388 intron variant C/A snv 0.14 0.010 1.000 1 2017 2017
dbSNP: rs2234767
rs2234767
ACTA2 ; FAS
30 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 0.010 1.000 1 2018 2018
dbSNP: rs2292657
rs2292657
GLI1
1 1.000 0.040 12 57466149 intron variant G/A snv 0.48 0.010 1.000 1 2013 2013
dbSNP: rs4076018
rs4076018
NGF ; NGF-AS1
1 1.000 0.040 1 115300189 intron variant A/T snv 0.25 0.010 1.000 1 2013 2013
dbSNP: rs422342
rs422342
LOC102723493
1 1.000 0.040 15 67055348 intron variant A/G snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs470859
rs470859
GLT1D1
1 1.000 0.040 12 128912087 intron variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs4875102
rs4875102
CSMD1
1 1.000 0.040 8 4427170 intron variant G/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs5030772
rs5030772
FASLG
7 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 0.010 1.000 1 2018 2018
dbSNP: rs7975253
rs7975253
ANAPC5
1 1.000 0.040 12 121375864 intron variant C/T snv 6.8E-02 0.010 1.000 1 2017 2017
dbSNP: rs926849
rs926849
PRKN
1 1.000 0.040 6 161740587 intron variant C/T snv 0.67 0.800 1.000 1 2013 2013
dbSNP: rs9301951
rs9301951
GPC6
1 1.000 0.040 13 94300578 intron variant T/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs10214886
rs10214886 		1 1.000 0.040 6 32889642 intergenic variant T/A snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs1029295
rs1029295 		1 1.000 0.040 6 32888705 intergenic variant T/C snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs1029296
rs1029296 		1 1.000 0.040 6 32888604 intergenic variant T/C snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs17034687
rs17034687 		1 1.000 0.040 3 3638168 intergenic variant C/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs2187689
rs2187689 		1 1.000 0.040 6 32884870 intergenic variant T/C snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs6457690
rs6457690 		1 1.000 0.040 6 32887940 intergenic variant G/A snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs6936004
rs6936004 		1 1.000 0.040 6 32889157 intergenic variant T/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs10046257
rs10046257 		1 1.000 0.040 6 32886920 regulatory region variant G/A snv 0.15 0.800 1.000 1 2013 2013
dbSNP: rs17576
rs17576
MMP9
73 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.020 1.000 2 2017 2018