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: rs28928891
rs28928891
HOXD13
2 1.000 0.080 2 176094662 missense variant A/C;G snv 8.0E-06 0.800 1.000 2 2003 2014
dbSNP: rs28928892
rs28928892
HOXD13
2 1.000 0.080 2 176094645 missense variant C/A;G snv 4.0E-06 0.800 1.000 2 2003 2014
dbSNP: rs1555429629
rs1555429629
RAD51
23 0.763 0.200 15 40729632 missense variant G/A snv 0.700 0