STOX1, storkhead box 1, 219736

N. diseases: 39; N. variants: 15
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10082399
rs10082399
1.000 0.040 10 68872027 intron variant G/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1163174
rs1163174
10 68847824 intron variant T/C snv 0.54
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1417941
rs1417941
1.000 0.040 10 68859103 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs41278532
rs41278532
1.000 0.040 10 68886270 missense variant A/T snv 2.7E-03 2.4E-03
CUI: C1836255
Disease: Preeclampsia Eclampsia 4
Preeclampsia Eclampsia 4
Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2005 2005
dbSNP: rs4320849
rs4320849
1.000 0.040 10 68861330 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4746797
rs4746797
1.000 0.040 10 68871873 intron variant T/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs556362193
rs556362193
1.000 0.040 10 68827676 missense variant G/C;T snv 1.0E-02
CUI: C1836255
Disease: Preeclampsia Eclampsia 4
Preeclampsia Eclampsia 4
Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2005 2005
dbSNP: rs7083105
rs7083105
1.000 0.040 10 68862365 intron variant C/T snv 2.8E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10509305
rs10509305
1.000 0.040 10 68885620 missense variant A/C;T snv 0.22; 4.0E-06
CUI: C1836255
Disease: Preeclampsia Eclampsia 4
Preeclampsia Eclampsia 4
Female Urogenital Diseases and Pregnancy Complications 0.700 0
dbSNP: rs1341667
rs1341667
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57
CUI: C1836255
Disease: Preeclampsia Eclampsia 4
Preeclampsia Eclampsia 4
Female Urogenital Diseases and Pregnancy Complications 0.700 0
dbSNP: rs1341667
rs1341667
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57
CUI: C0013537
Disease: Eclampsia
Eclampsia
Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2010 2011
dbSNP: rs10998461
rs10998461
1.000 0.080 10 68856761 intron variant G/T snv 0.44
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.010 1.000 1 2020 2020
dbSNP: rs10998468
rs10998468
1.000 0.080 10 68867495 intron variant T/C snv 0.22
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.010 1.000 1 2020 2020
dbSNP: rs1341667
rs1341667
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57
CUI: C0015934
Disease: Fetal Growth Retardation
Fetal Growth Retardation
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2007 2007
dbSNP: rs1341667
rs1341667
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2010 2010
dbSNP: rs1417939
rs1417939
0.925 0.080 10 68874648 intron variant G/A snv 0.73
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1417939
rs1417939
0.925 0.080 10 68874648 intron variant G/A snv 0.73
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4472827
rs4472827
1.000 0.080 10 68892516 intron variant G/A snv 0.33
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.010 1.000 1 2020 2020
dbSNP: rs7903209
rs7903209
1.000 0.080 10 68868826 intron variant C/T snv 0.28
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.010 1.000 1 2020 2020