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: rs10083777
rs10083777
CENPN ; LOC107984858
2 16 81031677 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs1009714
rs1009714
KTN1-AS1
1 14 55512820 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1009977
rs1009977
LGALS3
2 1.000 0.040 14 55136284 intron variant T/G snv 0.48 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: rs10129505
rs10129505
FBXO34
1 14 55309657 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10131232
rs10131232
GCH1
1 14 54849190 intron variant G/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10131730
rs10131730
ATG14
1 14 55373374 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10133662
rs10133662
GCH1
1 14 54849552 intron variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10134019
rs10134019
KTN1-AS1
1 14 55530274 intron variant T/G snv 0.54 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: rs10134339
rs10134339
FBXO34
1 14 55347662 intron variant T/C snv 0.57 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: rs10137307
rs10137307
ATG14
1 14 55378467 intron variant T/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10139354
rs10139354
WDHD1
1 14 55011884 intron variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs10140801
rs10140801
LOC105370509
1 14 55263686 intron variant C/T snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs10140857
rs10140857
DLGAP5
1 14 55152893 intron variant G/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs10140869
rs10140869
FBXO34
1 14 55328565 intron variant G/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10141396
rs10141396
FBXO34
1 14 55350207 intron variant T/G snv 0.30 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: rs10142448
rs10142448
ATG14
1 14 55371390 intron variant A/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs10146637
rs10146637
FBXO34
2 14 55278092 intron variant G/A snv 0.30 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