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: rs11119328
rs11119328
HSD11B1 ; HSD11B1-AS1
1 1.000 1 209711973 intron variant C/A;T snv 0.010 1.000 1 2020 2020
dbSNP: rs11811440
rs11811440
HSD11B1 ; HSD11B1-AS1
1 1.000 1 209709555 intron variant C/A;T snv 0.010 1.000 1 2020 2020