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: rs1002054
rs1002054
MAPK1IP1L
1 14 55062195 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1009714
rs1009714
KTN1-AS1
1 14 55512820 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1009978
rs1009978
LGALS3
1 14 55136343 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134317
rs10134317
FBXO34
1 14 55326730 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134800
rs10134800
DLGAP5
1 14 55168491 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134983
rs10134983
DLGAP5
1 14 55168605 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10136596
rs10136596
ATG14
1 14 55370055 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10138446
rs10138446
ATG14
1 14 55412967 upstream gene variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10141552
rs10141552
FBXO34
1 14 55279373 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10146736
rs10146736
TBPL2 ; LOC107984664
1 14 55431206 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10147765
rs10147765
FBXO34
1 14 55361108 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10265221
rs10265221
PRKAG2
3 7 151717243 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs1045002
rs1045002
FBXO34
1 14 55351799 missense variant T/A;G snv 0.38; 4.0E-05 0.700 1.000 1 2012 2012
dbSNP: rs1045004
rs1045004
FBXO34
1 14 55353073 3 prime UTR variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10498472
rs10498472
GCH1
1 14 54888151 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1187883
rs1187883
WDHD1
1 14 55021516 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1188074
rs1188074
KTN1-AS1
1 14 55505113 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1201378
rs1201378
WDHD1 ; SOCS4
1 14 55026690 intron variant T/A;C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1209087
rs1209087
WDHD1 ; SOCS4
1 14 55026502 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1212641
rs1212641
SOCS4
1 14 55029413 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12587434
rs12587434
GCH1
1 14 54858865 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1307315
rs1307315
KTN1-AS1
1 14 55501077 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1538257
rs1538257
ATG14
1 14 55412559 upstream gene variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs15870
rs15870
DLGAP5
1 14 55152593 missense variant A/G;T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs17128120
rs17128120
WDHD1
1 14 55007880 intron variant C/G;T snv 0.700 1.000 1 2012 2012