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: rs33980500
rs33980500
TRAF3IP2 ; TRAF3IP2-AS1
14 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 0.820 1.000 4 2010 2015
dbSNP: rs13017599
rs13017599
NONOP2
3 0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 0.810 1.000 3 2012 2015
dbSNP: rs702873
rs702873
LINC01185
3 0.882 0.120 2 60854407 intron variant C/T snv 0.35 0.810 1.000 1 2012 2012
dbSNP: rs12188300
rs12188300 		6 0.807 0.120 5 159402519 intron variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs13191343
rs13191343
HLA-B ; HLA-C
1 1.000 0.080 6 31273332 intron variant C/G;T snv 0.13 0.800 1.000 1 2010 2010
dbSNP: rs13190932
rs13190932
TRAF3IP2 ; TRAF3IP2-AS1
1 1.000 0.080 6 111591867 missense variant G/A snv 5.3E-02 5.0E-02 0.710 1.000 2 2010 2019
dbSNP: rs12044149
rs12044149
C1orf141
2 0.925 0.080 1 67135003 intron variant G/C;T snv 0.710 1.000 1 2015 2015
dbSNP: rs10865331
rs10865331 		5 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs114212579
rs114212579
CYP21A2 ; SKIV2L
1 1.000 0.080 6 31968280 non coding transcript exon variant G/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114265779
rs114265779
TRIM26
1 1.000 0.080 6 30213844 upstream gene variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114383947
rs114383947
MUC22
1 1.000 0.080 6 31010940 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114598684
rs114598684
MICA
1 1.000 0.080 6 31413173 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114757170
rs114757170
PPP1R10 ; MRPS18B
1 1.000 0.080 6 30618254 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs115112280
rs115112280
HCG23 ; TSBP1-AS1
1 1.000 0.080 6 32390772 non coding transcript exon variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs115145466
rs115145466 		1 1.000 0.080 6 32251264 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115429782
rs115429782
HLA-B ; LINC02571 ; LOC112267902
1 1.000 0.080 6 31297975 intron variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs115429849
rs115429849
MICC
1 1.000 0.080 6 30416827 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs115529844
rs115529844
LOC105375010
1 1.000 0.080 6 29850244 non coding transcript exon variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs115618145
rs115618145
TRIM31
1 1.000 0.080 6 30102498 upstream gene variant C/G snv 0.700 1.000 1 2019 2019
dbSNP: rs115645848
rs115645848
GABBR1
1 1.000 0.080 6 29622938 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115872194
rs115872194
BAG6
1 1.000 0.080 6 31639897 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115928623
rs115928623
HLA-A ; MICD
1 1.000 0.080 6 29971371 intron variant A/T snv 0.700 1.000 1 2019 2019
dbSNP: rs116199901
rs116199901
HCG18 ; HCG17
1 1.000 0.080 6 30315875 intron variant G/C snv 0.700 1.000 1 2019 2019
dbSNP: rs116340302
rs116340302
MCCD1 ; RPL15P4
1 1.000 0.080 6 31528604 non coding transcript exon variant A/T snv 0.700 1.000 1 2019 2019
dbSNP: rs116805908
rs116805908
POU5F1 ; PSORS1C3
1 1.000 0.080 6 31173746 non coding transcript exon variant C/T snv 0.700 1.000 1 2019 2019