rs786204858, PTEN

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
PTEN Hamartoma Tumor Syndrome
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
194 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 1.000 5 2013 2018
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Autistic behavior
CUI: C0856975
Disease: Autistic behavior
78 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Congenital pectus excavatum
CUI: C0016842
Disease: Congenital pectus excavatum
36 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
116 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Oral wart
CUI: C1262299
Disease: Oral wart
1 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Penile freckling
CUI: C4531112
Disease: Penile freckling
11 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0