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: rs62158211
rs62158211
LOC101927400
2 2 113348562 intron variant G/T snv 0.18 0.700 1.000 4 2016 2018
dbSNP: rs113851554
rs113851554
MEIS1
4 0.882 0.080 2 66523432 intron variant G/A;T snv 0.700 1.000 2 2017 2018
dbSNP: rs13109404
rs13109404
BANK1
1 4 101975434 intron variant T/G snv 4.1E-02 0.700 1.000 2 2019 2019
dbSNP: rs1553132
rs1553132
GRM5
1 11 88564572 intron variant A/G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs365663
rs365663
SLC6A3
1 5 1428768 intron variant A/G snv 0.54 0.700 1.000 2 2019 2019
dbSNP: rs4767550
rs4767550
KSR2 ; LOC105370012
1 12 117513345 intron variant A/G snv 0.33 0.700 1.000 2 2019 2019
dbSNP: rs61980273
rs61980273
PRIMA1
1 14 93752603 intron variant G/A snv 2.5E-02 0.700 1.000 2 2017 2017
dbSNP: rs7556815
rs7556815
LOC101927400
1 2 113328208 intron variant G/A snv 0.19 0.700 1.000 2 2018 2019
dbSNP: rs10483350
rs10483350
LOC102724934
1 14 29346949 intron variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs10761674
rs10761674
EGR2
1 10 62858580 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10953765
rs10953765
FOXP2 ; MIR3666
1 7 114651380 intron variant G/A snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs10987006
rs10987006
PBX3
1 9 125889260 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs11076146
rs11076146
GNAO1
1 16 56227517 intron variant T/G snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs11190970
rs11190970
BTRC
1 10 101368575 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs112230981
rs112230981
ERC2
1 3 55845241 intron variant A/G snv 2.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs112477743
rs112477743 		1 6 98202301 intron variant T/-;TT;TTT;TTTTTTTTTTT delins 0.700 1.000 1 2018 2018
dbSNP: rs113113059
rs113113059
CUL9
1 6 43192637 intron variant T/C snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs113322698
rs113322698
KDM3B
1 5 138433887 intron variant G/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs115419280
rs115419280
TNIK ; LOC105374216
1 3 171131724 intron variant A/C snv 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs11567976
rs11567976
CDC25C
1 5 138318529 intron variant C/T snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs11602180
rs11602180
PTPRJ
1 11 48140901 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs11614986
rs11614986
MMAB
1 12 109570134 intron variant A/G snv 0.15 0.17 0.700 1.000 1 2019 2019
dbSNP: rs116219610
rs116219610
LINC01122
1 2 58622593 intron variant C/G;T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs11650677
rs11650677
SHISA6
1 17 11328196 intron variant G/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs11682175
rs11682175
ACTG1P22
4 0.925 0.040 2 57760458 intron variant T/C snv 0.38 0.700 1.000 1 2019 2019