Source: GWASCAT ×
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: rs10484399
rs10484399 		1 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs11244
rs11244
HLA-DOB
1 0.925 0.160 6 32812947 3 prime UTR variant G/A snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs1265757
rs1265757
TSBP1 ; TSBP1-AS1
1 1.000 0.040 6 32334605 intron variant C/T snv 6.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs13213152
rs13213152
ZSCAN12
1 1.000 0.040 6 28381921 3 prime UTR variant A/G snv 5.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs1633005
rs1633005
HLA-V
1 1.000 0.040 6 29796695 non coding transcript exon variant C/A;T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs1953600
rs1953600
ANXA11
1 1.000 0.040 10 80151969 3 prime UTR variant C/T snv 0.37 0.800 1.000 1 2008 2013
dbSNP: rs1964995
rs1964995 		1 0.925 0.160 6 32481634 intergenic variant T/C snv 0.34 0.800 1.000 1 2012 2016
dbSNP: rs2076530
rs2076530
BTNL2 ; TSBP1-AS1
1 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 0.900 0.933 1 2005 2019
dbSNP: rs2233974
rs2233974
C6orf15
1 1.000 0.040 6 31112239 missense variant C/A;G snv 4.0E-06; 0.14 0.700 1.000 1 2016 2016
dbSNP: rs223498
rs223498
MANBA
1 1.000 0.040 4 102730805 intron variant A/C snv 0.59 0.700 1.000 1 2015 2015
dbSNP: rs2524067
rs2524067
HLA-B ; USP8P1
1 1.000 0.040 6 31278044 non coding transcript exon variant A/G snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs2847260
rs2847260 		1 1.000 0.040 18 12775592 non coding transcript exon variant C/T snv 0.82 0.700 1.000 1 2015 2015
dbSNP: rs3129788
rs3129788 		1 1.000 0.040 6 29089862 upstream gene variant G/A snv 5.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs3130141
rs3130141
LOC105375012
1 1.000 0.040 6 30464400 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3130288
rs3130288
ATF6B ; FKBPL
1 1.000 0.040 6 32128224 5 prime UTR variant C/A;G snv 5.9E-02; 4.1E-06 0.700 1.000 1 2016 2016
dbSNP: rs3130662
rs3130662
IER3
1 1.000 0.040 6 30746031 intron variant C/A snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs3130895
rs3130895 		1 1.000 0.040 6 28938014 intergenic variant G/A snv 5.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs479777
rs479777
CCDC88B ; LOC102723878
1 1.000 0.040 11 64340005 upstream gene variant T/C snv 0.27 0.810 1.000 1 2012 2012
dbSNP: rs4921492
rs4921492 		1 0.925 0.120 5 159405269 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs6748088
rs6748088
FAM117B
1 1.000 0.040 2 202691803 intron variant T/C snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs886420
rs886420
GTF2H4
1 1.000 0.040 6 30911859 non coding transcript exon variant C/T snv 7.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs915652
rs915652
VARS1
1 1.000 0.040 6 31781365 non coding transcript exon variant G/A snv 6.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs9275582
rs9275582 		1 0.925 0.160 6 32712293 regulatory region variant C/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs933957
rs933957
SP140
1 1.000 0.040 2 230313189 3 prime UTR variant T/C snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs12069782
rs12069782
C1orf141
2 1.000 0.040 1 67134418 intron variant C/T snv 0.82 0.700 1.000 1 2015 2015