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: rs10023335
rs10023335
SHROOM3
4 76437834 intron variant T/C snv 0.29
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0.700 1.000 1 2019 2019
dbSNP: rs9992101
rs9992101
SHROOM3
4 76439278 intron variant G/A snv 0.28
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2010 2010
dbSNP: rs55940751
rs55940751
SHROOM3
4 76444738 intron variant C/T snv 0.32
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs568240689
rs568240689
SHROOM3
4 76445096 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
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: rs17319721
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.800 1.000 1 2013 2016
dbSNP: rs17319721
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.700 1.000 1 2010 2010
dbSNP: rs2870238
rs2870238
SHROOM3
4 76451926 intron variant C/T snv 0.39
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2870238
rs2870238
SHROOM3
4 76451926 intron variant C/T snv 0.39
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10032549
rs10032549
SHROOM3
4 76476862 intron variant A/G snv 0.43
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.800 1.000 1 2013 2013
dbSNP: rs111449836
rs111449836
SHROOM3
4 76480299 intron variant C/T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs28817415
rs28817415
SHROOM3
1.000 0.080 4 76480299 intron variant C/T snv 0.33
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs28817415
rs28817415
SHROOM3
1.000 0.080 4 76480299 intron variant C/T snv 0.33
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs28817415
rs28817415
SHROOM3
1.000 0.080 4 76480299 intron variant C/T snv 0.33
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.700 1.000 1 2019 2019
dbSNP: rs7654754
rs7654754
SHROOM3
4 76488642 intron variant G/A snv 0.43
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.700 1.000 1 2018 2018
dbSNP: rs4859682
rs4859682
SHROOM3
4 76489165 intron variant C/A snv 0.33
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.800 1.000 1 2013 2013
dbSNP: rs4859682
rs4859682
SHROOM3
4 76489165 intron variant C/A snv 0.33
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13146355
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 3 2017 2019
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: rs13146355
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs13146355
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0373675
Disease: Magnesium measurement
Magnesium measurement 		0.800 1.000 1 2010 2010
dbSNP: rs13146355
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2019 2019
dbSNP: rs13146355
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2019 2019
dbSNP: rs7675258
rs7675258
SHROOM3
4 76492026 intron variant G/A snv 0.44
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs10008637
rs10008637
SHROOM3
4 76492991 intron variant T/A;C snv 0.35
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019