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: rs1403898124
rs1403898124
RARA
1 1.000 0.080 17 40356141 missense variant G/A snv 6.5E-06 0.010 1.000 1 2015 2015
dbSNP: rs28934578
rs28934578
TP53
47 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs41293463
rs41293463
BRCA1
9 0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 0.010 1.000 1 2011 2011
dbSNP: rs762374504
rs762374504
RARA
1 1.000 0.080 17 40354432 missense variant C/T snv 4.0E-06 0.010 1.000 1 2015 2015