Gene: ERAP1 ×
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: rs27524
rs27524
CAST ; ERAP1
4 0.851 0.160 5 96766240 intron variant A/G snv 0.61 0.800 1.000 2 2010 2015
dbSNP: rs27432
rs27432
ERAP1 ; LOC102724748
2 0.925 0.040 5 96783569 intron variant A/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs27044
rs27044
ERAP1 ; LOC102724748
5 0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 0.710 1.000 2 2015 2017
dbSNP: rs2910686
rs2910686
ERAP1 ; ERAP2
5 0.827 0.120 5 96916885 intron variant T/C snv 0.42 0.700 1.000 2 2012 2016
dbSNP: rs151823
rs151823
ERAP1
1 1.000 0.040 5 96824289 intron variant A/C snv 0.90 0.700 1.000 1 2010 2010
dbSNP: rs2549803
rs2549803
ERAP1
5 0.827 0.120 5 96839226 intron variant C/T snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs39841
rs39841
ERAP1 ; LOC102724748
1 1.000 0.040 5 96784466 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs469758
rs469758
ERAP1 ; LOC102724748
5 0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63 0.700 1.000 1 2016 2016
dbSNP: rs4869313
rs4869313
ERAP1 ; ERAP2
14 0.724 0.240 5 96888176 intron variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs26653
rs26653
ERAP1
4 0.882 0.080 5 96803547 missense variant C/A;G;T snv 0.64; 8.0E-06; 9.1E-04 0.020 0.500 2 2013 2018
dbSNP: rs30187
rs30187
ERAP1
14 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 0.010 1.000 1 2017 2017