Source: ALL
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: rs764256352
rs764256352
SLC26A2
3 0.882 0.120 5 149981625 missense variant G/C snv 4.0E-06 2.1E-05 0.010 1.000 1 2019 2019