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: rs770727871
rs770727871
NTRK1
1 1.000 0.080 1 156880092 missense variant G/A snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs786205449
rs786205449
NTRK1
1 1.000 0.080 1 156879262 missense variant G/A snv 0.700 0
dbSNP: rs80356673
rs80356673
INSRR ; NTRK1
1 1.000 0.080 1 156860959 stop gained C/A;T snv 0.700 0
dbSNP: rs80356674
rs80356674
NTRK1
1 1.000 0.080 1 156873600 intron variant T/A snv 3.4E-05 0.700 0
dbSNP: rs80356675
rs80356675
NTRK1
1 1.000 0.080 1 156876427 frameshift variant C/- del 0.700 0
dbSNP: rs80356676
rs80356676
NTRK1
1 1.000 0.080 1 156879176 frameshift variant -/T ins 0.700 0
dbSNP: rs879253889
rs879253889
NTRK1
1 1.000 0.080 1 156868201 stop gained C/T snv 0.700 0