rs111033220, SLC26A4

N. diseases: 4
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.
Pendred's syndrome
CUI: C0271829
Disease: Pendred's syndrome
142 0.925 0.160 7 107690203 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.800 1.000 36 1997 2017
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
81 0.925 0.160 7 107690203 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.800 1.000 33 1998 2019
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 0.925 0.160 7 107690203 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.700 0
Hearing Loss
CUI: C3887873
Disease: Hearing Loss
61 0.925 0.160 7 107690203 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.700 0