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: rs28933082
rs28933082
HOXD13
2 0.925 0.080 2 176094614 missense variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs879255265
rs879255265
HOXD13
2 0.925 0.080 2 176094615 missense variant G/A snv 0.010 1.000 1 2014 2014