Gene: INSIG2 ×
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: rs1412088853
rs1412088853
INSIG2
1 1.000 0.080 2 118108315 missense variant A/G snv 0.010 1.000 1 2011 2011
dbSNP: rs9308762
rs9308762
INSIG2
2 0.925 0.120 2 118106298 intron variant C/A;G;T snv 0.010 1.000 1 2014 2014