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: rs121909174
rs121909174
SLC5A5
3 0.925 0.120 19 17881961 missense variant A/C snv 1.2E-05 0.800 1.000 4 1997 1999
dbSNP: rs121909176
rs121909176
SLC5A5
1 1.000 0.120 19 17877823 missense variant C/G snv 8.4E-05 2.8E-05 0.800 1.000 4 1997 1999
dbSNP: rs121909178
rs121909178
SLC5A5
1 1.000 0.120 19 17872596 missense variant G/A;C snv 0.800 1.000 4 1997 1999
dbSNP: rs121909179
rs121909179
SLC5A5
1 1.000 0.120 19 17888432 missense variant G/A snv 0.800 1.000 4 1997 1999
dbSNP: rs121909180
rs121909180
SLC5A5
1 1.000 0.120 19 17882160 missense variant G/A snv 4.0E-05 2.1E-05 0.800 1.000 4 1997 1999
dbSNP: rs121909175
rs121909175
SLC5A5
2 0.925 0.120 19 17877840 stop gained C/A snv 7.0E-06 0.700 0
dbSNP: rs121909177
rs121909177
SLC5A5
1 1.000 0.120 19 17888397 stop gained C/G;T snv 5.6E-05; 2.0E-05 0.700 0