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: rs9895661
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 5 2010 2018
dbSNP: rs2279463
rs2279463
SLC22A2
1.000 0.080 6 160247357 intron variant A/G;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 4 2010 2019
dbSNP: rs2453533
rs2453533 		1.000 0.080 15 45349027 intergenic variant C/A snv 0.56
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 3 2010 2017
dbSNP: rs3925584
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 3 2016 2019
dbSNP: rs77924615
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 3 2017 2019
dbSNP: rs881858
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 3 2010 2018
dbSNP: rs10109414
rs10109414 		1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs10774021
rs10774021
SLC6A13
1.000 0.080 12 240132 intron variant C/T snv 0.57
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs10794720
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs11959928
rs11959928
C9 ; DAB2
1.000 0.080 5 39397030 intron variant T/A snv 0.39
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs12460876
rs12460876
SLC7A9
1.000 0.080 19 32865985 intron variant T/C snv 0.36
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs12917707
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs13146355
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2017 2019
dbSNP: rs1394125
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs17319721
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs2467853
rs2467853
SPATA5L1
1.000 0.080 15 45406595 intron variant T/A;G snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2016 2019
dbSNP: rs267734
rs267734 		0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs347685
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs4014195
rs4014195 		0.882 0.200 11 65739351 intergenic variant C/G snv 0.31
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
dbSNP: rs4744712
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 2 2010 2016
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