rs1564405163, GATA3

N. diseases: 6
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.
Barakat syndrome
CUI: C1840333
Disease: Barakat syndrome
9 0.807 0.280 10 8073746 missense variant G/C snv 0.700 0
Chronic kidney disease stage 2
CUI: C2316786
Disease: Chronic kidney disease stage 2
1 0.807 0.280 10 8073746 missense variant G/C snv 0.700 0
Hypoparathyroidism
CUI: C0020626
Disease: Hypoparathyroidism
15 0.807 0.280 10 8073746 missense variant G/C snv 0.700 0
Multicystic Dysplastic Kidney
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
11 0.807 0.280 10 8073746 missense variant G/C snv 0.700 0
Progressive sensorineural hearing impairment
CUI: C1843156
Disease: Progressive sensorineural hearing impairment
28 0.807 0.280 10 8073746 missense variant G/C snv 0.700 0
Sensorineural hearing loss, bilateral
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
30 0.807 0.280 10 8073746 missense variant G/C snv 0.700 0