Gene: INSR ×
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: rs121913139
rs121913139
INSR
2 1.000 0.120 19 7122662 missense variant C/T snv 0.700 0
dbSNP: rs121913157
rs121913157
INSR
1 19 7120739 missense variant C/T snv 0.700 0
dbSNP: rs1568426700
rs1568426700
INSR
1 19 7120678 missense variant G/A snv 0.700 0