Source: GWASDB ×
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: rs2866406
rs2866406
MANBA
1 1.000 0.080 4 102632862 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2866407
rs2866407
MANBA
1 1.000 0.080 4 102632951 intron variant C/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2866408
rs2866408
MANBA
1 1.000 0.080 4 102632956 intron variant T/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2866409
rs2866409
MANBA
1 1.000 0.080 4 102633104 intron variant T/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2866412
rs2866412
MANBA
1 1.000 0.080 4 102633193 intron variant T/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs12498722
rs12498722
MANBA
1 1.000 0.080 4 102633365 missense variant C/T snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs5026476
rs5026476
MANBA
1 1.000 0.080 4 102633753 intron variant A/C snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs13106304
rs13106304
MANBA
1 1.000 0.080 4 102633818 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs13106325
rs13106325
MANBA
1 1.000 0.080 4 102633835 intron variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6821119
rs6821119
MANBA
1 1.000 0.080 4 102634076 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs6844332
rs6844332
MANBA
1 1.000 0.080 4 102634095 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs6812747
rs6812747
MANBA
1 1.000 0.080 4 102634260 intron variant A/C snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs6813322
rs6813322
MANBA
1 1.000 0.080 4 102634462 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs6839064
rs6839064
MANBA
1 1.000 0.080 4 102634519 intron variant T/C snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2272695
rs2272695
MANBA
1 1.000 0.080 4 102634646 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2272696
rs2272696
MANBA
1 1.000 0.080 4 102634664 intron variant G/A snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs2866413
rs2866413
MANBA
1 1.000 0.080 4 102635920 missense variant G/A;C snv 0.54; 2.4E-05 0.700 1.000 2 2011 2012
dbSNP: rs228615
rs228615
MANBA
1 1.000 0.080 4 102658303 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs228616
rs228616
MANBA
1 1.000 0.080 4 102658534 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8017161
rs8017161
EXOC3L4
1 0.925 0.080 14 103096858 intron variant G/A snv 0.38 0.800 1.000 1 2011 2011
dbSNP: rs2297067
rs2297067
EXOC3L4
2 1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 0.800 1.000 1 2011 2015
dbSNP: rs34536443
rs34536443
TYK2
4 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs2304256
rs2304256
TYK2
3 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 0.800 1.000 1 2012 2015
dbSNP: rs805722
rs805722
COL17A1
1 1.000 0.080 10 104050642 missense variant T/A;C snv 8.0E-06; 0.78 0.700 1.000 1 2012 2012
dbSNP: rs11191909
rs11191909
COL17A1
1 1.000 0.080 10 104053243 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012