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: rs491567
rs491567
WDR72
1.000 0.080 15 53654396 intron variant A/C snv 0.34
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs626277
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs6420094
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs6465825
rs6465825 		1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs716877
rs716877
DACH1
13 71773316 intron variant C/G snv 0.43
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2016 2018
dbSNP: rs7247977
rs7247977
SLC7A9
19 32867449 intron variant T/C snv 0.46
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2017 2018
dbSNP: rs7422339
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs807601
rs807601 		2 15652890 intergenic variant G/T snv 0.48
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2016 2017
dbSNP: rs963837
rs963837
LINC02859 ; LOC101928338
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2016 2018
dbSNP: rs10062079
rs10062079
C9 ; DAB2
5 39393631 intron variant G/A snv 0.39
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs10127790
rs10127790
SORT1
1 109348511 intron variant C/T snv 0.63
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2017 2017
dbSNP: rs10206899
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2010 2010
dbSNP: rs10254101
rs10254101
PRKAG2
7 151718450 intron variant C/T snv 0.23
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2017 2017
dbSNP: rs10262995
rs10262995
BBS9
7 33510429 intron variant C/T snv 9.1E-02
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2015 2015
dbSNP: rs10277115
rs10277115 		7 1245559 regulatory region variant A/T snv 0.57
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1044261
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10459012
rs10459012 		11 55324098 upstream gene variant C/A snv 0.25
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs10491967
rs10491967
TSPAN9
12 3258927 intron variant G/A snv 0.21
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10513801
rs10513801
ETV5
3 186104564 intron variant T/G snv 9.2E-02
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10518732
rs10518732
WDR72
15 53646845 intron variant G/A;C snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs10518733
rs10518733
WDR72
15 53648110 intron variant A/C;G snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2010 2010
dbSNP: rs10746942
rs10746942
PIP5K1B
9 68819549 intron variant G/A snv 0.63
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2017 2017
dbSNP: rs10794486
rs10794486
IGF1R
15 98758306 intron variant G/A;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs10840341
rs10840341 		11 2095263 intergenic variant T/A;C snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs10851885
rs10851885
NRG4
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2017 2017