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: rs121909110
rs121909110
ESRRB
1 1.000 0.120 14 76439682 missense variant C/T snv 0.800 1.000 1 2008 2008
dbSNP: rs121909111
rs121909111
ESRRB
1 1.000 0.120 14 76491683 missense variant G/T snv 4.9E-06 0.800 1.000 1 2008 2008
dbSNP: rs201714970
rs201714970
ESRRB
1 1.000 0.120 14 76498322 missense variant C/A;T snv 1.2E-04 0.700 1.000 1 2008 2008
dbSNP: rs1060499794
rs1060499794
ESRRB
1 1.000 0.120 14 76482046 missense variant G/A snv 0.700 0
dbSNP: rs375916159
rs375916159
ESRRB
1 1.000 0.120 14 76482759 missense variant G/A;T snv 0.700 0