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: rs2395185
rs2395185
HLA-DRB9
17 0.724 0.360 6 32465390 intron variant G/T snv 0.29 0.710 1.000 2 2012 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
29 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 0.710 0.500 2 2011 2018
dbSNP: rs6904596
rs6904596
HNRNPA1P1
5 0.851 0.160 6 27523520 non coding transcript exon variant G/A snv 0.11 0.710 1.000 2 2012 2016
dbSNP: rs748404
rs748404
TGM5
4 0.851 0.160 15 43267033 upstream gene variant T/C snv 0.17 0.710 1.000 2 2009 2011
dbSNP: rs9387478
rs9387478
DCBLD1
4 0.851 0.080 6 117465017 intron variant C/A;T snv 0.710 1.000 2 2012 2016
dbSNP: rs36600
rs36600
MTMR3
5 0.827 0.080 22 29941597 intron variant T/C snv 0.78 0.710 1.000 1 2011 2011
dbSNP: rs11638372
rs11638372
CHRNB4 ; LOC112268142
5 0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 0.700 1.000 4 2008 2012
dbSNP: rs1394371
rs1394371 		4 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 0.700 1.000 4 2008 2012
dbSNP: rs1996371
rs1996371
CHRNB4 ; LOC112268142
4 1.000 0.080 15 78664464 intron variant T/C snv 0.28 0.700 1.000 4 2008 2012
dbSNP: rs4887077
rs4887077
CHRNB4 ; LOC112268142
4 1.000 0.080 15 78686022 intron variant C/T snv 0.28 0.700 1.000 4 2008 2012
dbSNP: rs6495314
rs6495314
CHRNB4 ; LOC112268142
4 0.925 0.080 15 78668187 intron variant A/C snv 0.35 0.700 1.000 4 2008 2012
dbSNP: rs13180
rs13180
IREB2
7 0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 0.700 1.000 3 2008 2012
dbSNP: rs3131379
rs3131379
MSH5 ; MSH5-SAPCD1
10 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 0.700 1.000 3 2008 2012
dbSNP: rs4887053
rs4887053 		4 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 0.700 1.000 3 2008 2012
dbSNP: rs1235162
rs1235162
GABBR1
6 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 0.700 1.000 2 2009 2012
dbSNP: rs12441998
rs12441998
CHRNB4
3 0.925 0.080 15 78637030 intron variant G/A snv 0.63 0.700 1.000 2 2009 2012
dbSNP: rs12594247
rs12594247
CHRNB4
3 0.925 0.080 15 78654291 intron variant C/T snv 0.14 0.700 1.000 2 2008 2012
dbSNP: rs1316971
rs1316971
CHRNB4
3 0.925 0.080 15 78638168 intron variant A/G;T snv 0.62 0.700 1.000 2 2009 2012
dbSNP: rs2187668
rs2187668
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 2 2009 2012
dbSNP: rs2734986
rs2734986
LOC105375010
5 0.827 0.160 6 29850791 intron variant T/C snv 0.10 0.700 1.000 2 2009 2012
dbSNP: rs3094054
rs3094054 		6 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 0.700 1.000 2 2009 2012
dbSNP: rs3099844
rs3099844
MICB-DT
13 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 0.700 1.000 2 2009 2012
dbSNP: rs3129791
rs3129791
HCG15
5 0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 0.700 1.000 2 2009 2012
dbSNP: rs3130350
rs3130350 		5 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 0.700 1.000 2 2009 2012
dbSNP: rs3130380
rs3130380
HCG18 ; HCG17
10 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 0.700 1.000 2 2009 2012