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: rs121908078
rs121908078
SLC26A2
2 0.925 0.120 5 149981128 missense variant C/A snv 4.8E-05 7.0E-06 0.700 0
dbSNP: rs104893915
rs104893915
SLC26A2
10 0.776 0.200 5 149980428 missense variant C/T snv 9.8E-04 1.0E-03 0.010 1.000 1 1997 1997
dbSNP: rs104893920
rs104893920
SLC26A2
3 0.882 0.120 5 149980866 missense variant A/G snv 0.010 1.000 1 1997 1997