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: rs10185316
rs10185316
INSIG2 ; LOC107985940
1 1.000 0.040 2 118086902 upstream gene variant C/G snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs11123469
rs11123469
INSIG2 ; LOC107985940
1 1.000 0.040 2 118086607 upstream gene variant T/C snv 0.14 0.010 1.000 1 2012 2012
dbSNP: rs1559509
rs1559509
INSIG2
1 1.000 0.040 2 118098351 intron variant G/A snv 0.25 0.010 1.000 1 2012 2012