Source: GWASCAT

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 100532732
Gene Symbol: MSH5-SAPCD1
MSH5-SAPCD1
MSH5-SAPCD1 readthrough (NMD candidate) 0.760 0.423
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
TSBP1 and BTNL2 antisense RNA 1 0.638 0.692
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 259197
Gene Symbol: NCR3
NCR3
natural cytotoxicity triggering receptor 3 0.638 0.769 3.7E-04
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
major histocompatibility complex, class I, B 0.379 0.885 3.9E-05
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 401247
Gene Symbol: LINC00243
LINC00243
long intergenic non-protein coding RNA 243 0.729 0.423
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 4439
Gene Symbol: MSH5
MSH5
mutS homolog 5 0.641 0.692 3.2E-11
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 9656
Gene Symbol: MDC1
MDC1
mediator of DNA damage checkpoint 1 0.628 0.692 2.3E-08
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 288
Gene Symbol: ANK3
ANK3
ankyrin 3 0.578 0.654 1.00
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
phenotype 0.120 None 1.000 1 1 2013 2016
Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
RNA binding fox-1 homolog 1 0.584 0.692 0.95
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 2 2 2013 2013
Entrez Id: 100506035
Gene Symbol: LINC00989
LINC00989
long intergenic non-protein coding RNA 989 0.890 0.115
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 1146
Gene Symbol: CHRNG
CHRNG
cholinergic receptor nicotinic gamma subunit 0.573 0.692 3.3E-19
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 2893
Gene Symbol: GRIA4
GRIA4
glutamate ionotropic receptor AMPA type subunit 4 0.631 0.615 1.8E-02
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 317761
Gene Symbol: C14orf39
C14orf39
chromosome 14 open reading frame 39 0.861 0.038 2.7E-06
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 388336
Gene Symbol: SHISA6
SHISA6
shisa family member 6 0.861 0.077 0.85
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
laminin subunit alpha 2 0.553 0.692 2.4E-47
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 4642
Gene Symbol: MYO1D
MYO1D
myosin ID 0.780 0.269 1.3E-12
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 5095
Gene Symbol: PCCA
PCCA
propionyl-CoA carboxylase subunit alpha 0.682 0.538 3.1E-15
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 55349
Gene Symbol: CHDH
CHDH
choline dehydrogenase 0.529 0.769 1.7E-06
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 55748
Gene Symbol: CNDP2
CNDP2
carnosine dipeptidase 2 0.659 0.500 1.0E-07
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 56479
Gene Symbol: KCNQ5
KCNQ5
potassium voltage-gated channel subfamily Q member 5 0.686 0.500 0.98
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 5801
Gene Symbol: PTPRR
PTPRR
protein tyrosine phosphatase receptor type R 0.743 0.346 8.7E-07
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 5923
Gene Symbol: RASGRF1
RASGRF1
Ras protein specific guanine nucleotide releasing factor 1 0.537 0.769 1.00
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 5959
Gene Symbol: RDH5
RDH5
retinol dehydrogenase 5 0.656 0.462 8.9E-11
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 6096
Gene Symbol: RORB
RORB
RAR related orphan receptor B 0.644 0.500 1.00
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2013 2013
Entrez Id: 729911
Gene Symbol: ANKRD34C-AS1
ANKRD34C-AS1
ANKRD34C antisense RNA 1 1.000
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
disease 0.100 None 1.000 1 1 2010 2010