Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs763006761
rs763006761
SLC26A4
0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		0.800 1.000 23 1997 2017
dbSNP: rs763006761
rs763006761
SLC26A4
0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		0.800 1.000 14 1998 2017
dbSNP: rs763006761
rs763006761
SLC26A4
0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.700 0