Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10157710
rs10157710
1 47496019 downstream gene variant C/T snv 0.78
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs11162351
rs11162351
AK5
1 77479047 intron variant C/G snv 0.31
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs11264327
rs11264327
1 155122631 downstream gene variant G/A;C;T snv
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs12032996
rs12032996
1 33454985 intergenic variant G/A snv 0.12
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs12727104
rs12727104
1 171454028 intergenic variant G/A snv 8.3E-02
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs12727980
rs12727980
1 200289967 intron variant C/T snv 0.54
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs10207567
rs10207567
2 202850250 intron variant G/A;C snv
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs1047891
rs1047891
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs13394343
rs13394343
2 85527219 intergenic variant C/A;T snv
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs183131780
rs183131780
2 225820170 intergenic variant C/T snv 1.0E-03
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs185291443
rs185291443
2 226120788 intergenic variant C/A;G snv
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2019 2019
dbSNP: rs34823645
rs34823645
2 227647210 intron variant T/C snv 3.9E-04
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2019 2019
dbSNP: rs35311980
rs35311980
2 228295484 intergenic variant C/T snv 4.9E-05
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2019 2019
dbSNP: rs35483183
rs35483183
2 227011971 intron variant G/A snv 8.4E-02
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs35924503
rs35924503
2 228266570 intergenic variant T/C snv 1.5E-04
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs4665972
rs4665972
2 27375230 intron variant T/C snv 0.69
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs6712846
rs6712846
2 207024356 intergenic variant G/A snv 0.53
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs6750228
rs6750228
2 51084986 intron variant T/A snv 6.9E-02
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs112607182
rs112607182
3 170309619 downstream gene variant C/T snv 5.3E-02
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs6768627
rs6768627
3 46853886 intron variant C/T snv 0.13
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs189107782
rs189107782
4 189807855 intron variant C/T snv 1.5E-03
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs3805382
rs3805382
NMU
4 55605384 intron variant A/G snv 0.36 0.29
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs4109437
rs4109437
4 189848068 intron variant G/A;C snv
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2019 2019
dbSNP: rs6535594
rs6535594
4 148211605 intron variant G/A snv 0.54
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018
dbSNP: rs7654754
rs7654754
4 76488642 intron variant G/A snv 0.43
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.700 1.000 1 2018 2018