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: rs10093547
rs10093547
ZFHX4-AS1 ; LOC107986952
3 0.882 0.040 8 76562310 intron variant T/G snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs10102591
rs10102591 		3 0.882 0.040 8 80479448 intron variant G/T snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs10228836
rs10228836
SPATA48
3 0.882 0.040 7 50136567 intron variant A/G snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10424978
rs10424978 		4 0.851 0.080 19 4837545 upstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10425559
rs10425559 		7 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 0.700 1.000 1 2016 2016
dbSNP: rs1050529
rs1050529
HLA-B ; MIR6891
3 0.882 0.040 6 31356838 missense variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs10810657
rs10810657 		7 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 2 2016 2019
dbSNP: rs10896064
rs10896064
EFEMP2
3 0.882 0.040 11 65873562 5 prime UTR variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs109077
rs109077
PPARGC1B
3 0.882 0.040 5 149817119 intron variant T/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs10995255
rs10995255
ZNF365 ; LOC105378327
3 0.882 0.040 10 62642673 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs11170164
rs11170164
KRT5
6 0.827 0.120 12 52519884 missense variant C/T snv 5.7E-02 5.3E-02 0.700 1.000 3 2015 2019
dbSNP: rs1126809
rs1126809
TYR ; LOC107984363
29 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 0.700 1.000 2 2016 2019
dbSNP: rs11719821
rs11719821
LPP
3 0.882 0.040 3 188370530 intron variant T/C snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs11741260
rs11741260
FGF10-AS1
3 0.882 0.040 5 44411963 intron variant G/A;C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs117744081
rs117744081
CPVL
4 0.851 0.080 7 29092663 missense variant A/G snv 2.2E-02 2.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs11993814
rs11993814 		3 0.882 0.040 8 80477556 intron variant C/T snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs12070203
rs12070203 		3 0.882 0.040 1 228858641 downstream gene variant C/T snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs12203592
rs12203592
IRF4
38 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2019
dbSNP: rs12205199
rs12205199 		3 0.882 0.040 6 150032420 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12210050
rs12210050
LOC105374875
8 0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 0.700 1.000 2 2011 2016
dbSNP: rs12466910
rs12466910 		3 0.882 0.040 2 11386590 downstream gene variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1246946
rs1246946 		4 0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs125124
rs125124
LINC-PINT ; LINC00513
3 0.882 0.040 7 130899925 intron variant C/G snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs12916300
rs12916300
HERC2
13 0.742 0.080 15 28165345 intron variant C/T snv 0.50 0.700 1.000 2 2016 2019
dbSNP: rs13014235
rs13014235
FLACC1
5 0.851 0.040 2 201350769 missense variant C/G snv 0.62 0.63 0.700 1.000 1 2015 2015