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: rs148172770
rs148172770
SHROOM3
4 76730805 missense variant C/T snv 1.3E-04 3.4E-04
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2018 2018
dbSNP: rs1013105
rs1013105
SHROOM3
4 76687512 intron variant G/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs143141511
rs143141511
SHROOM3
4 76647838 intron variant G/A snv 4.2E-03
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6838801
rs6838801
SHROOM3 ; LOC105377290
0.925 0.120 4 76628406 intron variant G/T snv 0.29
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.700 1.000 1 2017 2017
dbSNP: rs6838801
rs6838801
SHROOM3 ; LOC105377290
0.925 0.120 4 76628406 intron variant G/T snv 0.29
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.700 1.000 1 2017 2017
dbSNP: rs3923380
rs3923380
SHROOM3
1.000 0.080 4 76547441 intron variant C/A;T snv
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		0.700 1.000 1 2016 2016
dbSNP: rs6810716
rs6810716
SHROOM3
1.000 0.040 4 76530998 intron variant C/T snv 0.54
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10050141
rs10050141
SHROOM3
1.000 0.040 4 76530384 intron variant G/A snv 9.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4241595
rs4241595
SHROOM3
1.000 0.040 4 76527867 intron variant A/G snv 0.73
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13105942
rs13105942
SHROOM3
1.000 0.040 4 76527447 intron variant G/A snv 7.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13151434
rs13151434
SHROOM3
1.000 0.040 4 76527046 intron variant G/A snv 6.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6854652
rs6854652
SHROOM3
1.000 0.040 4 76525752 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6848817
rs6848817
SHROOM3
1.000 0.040 4 76525528 intron variant A/C snv 0.59
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1986734
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1986734
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		0.700 1.000 1 2010 2010
dbSNP: rs1986734
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12500824
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12500824
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12500824
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs5020545
rs5020545
SHROOM3
4 76493835 intron variant C/T snv 0.36
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2016 2016
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
dbSNP: rs10008637
rs10008637
SHROOM3
4 76492991 intron variant T/A;C snv 0.35
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
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: 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