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: rs10032216
rs10032216
LOC107986195
3 4 148748354 intron variant T/A;C snv 0.800 1.000 2 2013 2017
dbSNP: rs10519227
rs10519227
FGF7 ; FAM227B
2 15 49454167 intron variant T/A snv 0.20 0.800 1.000 1 2013 2013
dbSNP: rs10799824
rs10799824
MICOS10 ; LOC105376817 ; LOC105376819
3 1 19514680 intron variant G/A snv 0.18 0.800 1.000 1 2013 2013
dbSNP: rs11026407
rs11026407
ANO5 ; LOC102723370
2 11 22083484 intron variant C/A snv 0.54 0.800 1.000 1 2014 2014
dbSNP: rs11624776
rs11624776 		3 14 93129246 regulatory region variant A/C;T snv 0.800 1.000 1 2013 2013
dbSNP: rs11755845
rs11755845
LINC01512
2 6 43937043 regulatory region variant C/T snv 0.21 0.800 1.000 1 2013 2013
dbSNP: rs12126655
rs12126655
VAV3
2 1 107814198 intron variant A/G snv 0.33 0.800 1.000 1 2014 2014
dbSNP: rs13015993
rs13015993
LOC101928278
2 2 216760800 intron variant G/A snv 0.64 0.800 1.000 1 2013 2013
dbSNP: rs1537424
rs1537424
LINC00609
3 1.000 0.040 14 36104812 intron variant C/T snv 0.49 0.800 1.000 1 2013 2013
dbSNP: rs1571583
rs1571583
GLIS3
2 9 4267209 intron variant A/G snv 0.77 0.800 1.000 1 2013 2013
dbSNP: rs17723470
rs17723470
PRDM11
2 11 45206016 intron variant C/T snv 0.21 0.800 1.000 1 2013 2013
dbSNP: rs17776563
rs17776563 		2 15 88575873 intergenic variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs2622590
rs2622590
XKR4
4 0.925 0.080 8 55445714 intron variant G/A snv 0.15 0.800 1.000 1 2014 2014
dbSNP: rs334699
rs334699
NFIA
2 1 61154824 intron variant A/G snv 0.92 0.800 1.000 1 2013 2013
dbSNP: rs3813582
rs3813582
LINC01229 ; MAFTRR ; LOC105371356
3 16 79715456 non coding transcript exon variant T/C snv 0.28 0.800 1.000 1 2013 2013
dbSNP: rs4804416
rs4804416
INSR
3 19 7223837 intron variant T/G snv 0.37 0.800 1.000 1 2013 2013
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.800 1.000 1 2013 2013
dbSNP: rs6683419
rs6683419
MICOS10 ; LOC105376819
2 1 19501286 intron variant G/A snv 0.52 0.800 1.000 1 2014 2014
dbSNP: rs6885099
rs6885099
PDE8B
4 1.000 0.040 5 77234524 intron variant A/G snv 0.52 0.800 1.000 1 2013 2013
dbSNP: rs753760
rs753760
PDE10A
2 6 165632995 intron variant C/A;G snv 0.800 1.000 1 2013 2013
dbSNP: rs7825175
rs7825175
NRG1
2 8 32558756 intron variant G/A snv 0.18 0.800 1.000 1 2013 2013
dbSNP: rs925489
rs925489
PTCSC2
6 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 1 2014 2014
dbSNP: rs9472138
rs9472138
LOC107986598
6 0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 0.800 1.000 1 2013 2013
dbSNP: rs9497965
rs9497965
SASH1
3 1.000 0.040 6 148200156 regulatory region variant C/T snv 0.40 0.800 1.000 1 2013 2013
dbSNP: rs9915657
rs9915657
SOX9-AS1
2 17 72131395 intron variant T/A;C snv 0.800 1.000 1 2013 2013