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: rs2954021
rs2954021 		15 1.000 0.040 8 125469835 intron variant A/G snv 0.54 0.800 1.000 2 2011 2018
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.700 1.000 2 2008 2013
dbSNP: rs10091910
rs10091910
NCOA2
1 8 70196313 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10518765
rs10518765
UNC13C
3 1.000 0.040 15 54388434 intron variant A/C snv 0.16 0.700 1.000 1 2007 2007
dbSNP: rs10761779
rs10761779
JMJD1C
3 10 63515167 intron variant A/G snv 0.42 0.700 1.000 1 2008 2008
dbSNP: rs10822161
rs10822161
JMJD1C
1 10 63358443 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11216930
rs11216930
PHLDB1
2 1.000 0.040 11 118618067 intron variant A/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs11573824
rs11573824
TNFRSF11B
1 8 118947686 intron variant A/C;T snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs117047270
rs117047270
SLC26A4
1 7 107664388 intron variant T/A snv 3.3E-03 0.700 1.000 1 2018 2018
dbSNP: rs12197384
rs12197384
KIAA0319
1 6 24549087 intron variant C/T snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs12355784
rs12355784
JMJD1C
3 10 63361805 intron variant C/A;T snv 0.700 1.000 1 2008 2008
dbSNP: rs139089160
rs139089160
CDA
1 1 20592062 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs143370804
rs143370804
EIF4G3
1 1 21024072 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs144391488
rs144391488
BTNL2 ; TSBP1-AS1
1 6 32400783 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs150674717
rs150674717
ALDH5A1
1 6 24512970 intron variant G/A snv 2.0E-04 0.700 1.000 1 2018 2018
dbSNP: rs16856332
rs16856332
ABCB11
1 2 168984064 intron variant T/A;G snv 0.800 1.000 1 2011 2011
dbSNP: rs17689159
rs17689159
LINC01229 ; LOC105371356
1 16 79708493 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs1880887
rs1880887
PDZRN4
1 12 41327628 intron variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs1880889
rs1880889
PDZRN4
2 12 41327433 intron variant A/C snv 0.91 0.700 1.000 1 2013 2013
dbSNP: rs1883415
rs1883415
GPLD1
3 0.925 0.040 6 24491247 intron variant A/C snv 0.34 0.800 1.000 1 2011 2011
dbSNP: rs189263035
rs189263035
GPLD1
1 6 24489732 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2236653
rs2236653
ST3GAL4
1 11 126413890 intron variant C/T snv 0.45 0.800 1.000 1 2011 2011
dbSNP: rs2445752
rs2445752
CYP19A1 ; MIR4713HG
2 15 51284188 intron variant A/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs2519093
rs2519093
ABO
16 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs2593704
rs2593704
MGAT5
1 2 134247706 intron variant G/C snv 0.80 0.700 1.000 1 2018 2018