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: rs11190970
rs11190970
BTRC
1 10 101368575 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs1939455
rs1939455
TRPC6
1 11 101650155 intron variant G/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs13109404
rs13109404
BANK1
1 4 101975434 intron variant T/G snv 4.1E-02 0.700 1.000 2 2019 2019
dbSNP: rs13107325
rs13107325
SLC39A8
24 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs144625846
rs144625846
GBF1
1 10 102318287 intron variant A/G snv 9.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs17098961
rs17098961
MMP20 ; LOC101928477
1 11 102609659 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6889592
rs6889592
PAM
1 5 102978235 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs56372231
rs56372231
PAM
1 5 102986201 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs3776864
rs3776864
PAM
1 5 102992164 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs6979198
rs6979198
COG5
1 7 107557249 intron variant T/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs7778250
rs7778250
BCAP29
1 7 107584120 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7644809
rs7644809
LINC00635 ; LINC00636
1 3 107845612 non coding transcript exon variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs4402351
rs4402351 		1 12 107930149 intergenic variant A/G snv 0.20 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: rs16854
rs16854 		1 13 110103485 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs71440053
rs71440053
COL4A1
1 13 110177535 intron variant A/T snv 2.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs205024
rs205024
SHISA6
1 17 11324035 intron variant C/T snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs2863244
rs2863244
PAX8 ; PAX8-AS1
1 2 113243289 intron variant A/G snv 0.49 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: rs62158170
rs62158170
LOC101927400 ; LOC105373567
2 2 113324598 upstream gene variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs6737318
rs6737318
LOC101927400 ; LOC105373567
1 2 113325543 non coding transcript exon variant A/G snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs62158206
rs62158206
LOC101927400 ; LOC105373567
1 2 113327019 intron variant T/C snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs7556815
rs7556815
LOC101927400
1 2 113328208 intron variant G/A snv 0.19 0.700 1.000 2 2018 2019
dbSNP: rs2863957
rs2863957
LOC101927400
1 2 113331974 intron variant C/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs1823125
rs1823125
LOC101927400
1 2 113332835 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015