Source: CLINVAR ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs768471577
rs768471577
SLC26A4
1 0.925 0.160 7 107694476 missense variant A/G snv 7.6E-05 2.1E-05 0.710 1.000 7 2000 2015