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: rs545971
rs545971
ABO
8 9 133267960 intron variant T/A;C snv 0.700 1.000 2 2011 2012
dbSNP: rs6009
rs6009
F5
3 1.000 0.080 1 169529596 intron variant T/A;C snv 0.94 0.700 1.000 2 2011 2012
dbSNP: rs612169
rs612169
ABO
10 9 133268030 intron variant G/A snv 0.700 1.000 2 2011 2012
dbSNP: rs630014
rs630014
ABO
9 9 133274306 intron variant G/A;C snv 0.700 1.000 2 2011 2012
dbSNP: rs6427197
rs6427197
F5
2 1 169531352 intron variant C/A snv 0.92 0.700 1.000 2 2011 2012
dbSNP: rs643434
rs643434
ABO
8 9 133266942 intron variant A/G;T snv 0.700 1.000 2 2011 2012
dbSNP: rs644234
rs644234
ABO
7 9 133266804 intron variant G/T snv 0.700 1.000 2 2011 2012
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.700 1.000 2 2011 2012
dbSNP: rs674302
rs674302
ABO
8 9 133271249 intron variant A/T snv 0.700 1.000 2 2011 2012
dbSNP: rs7538157
rs7538157
BLZF1
1 1 169382306 intron variant A/C;G snv 5.9E-03; 6.2E-05 0.700 1.000 2 2011 2012
dbSNP: rs9797861
rs9797861
SLC44A2
9 0.790 0.200 19 10632450 intron variant C/A;G;T snv 0.710 1.000 2 2016 2016
dbSNP: rs10025152
rs10025152
F11-AS1
2 4 186304150 intron variant G/A snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs10029715
rs10029715
F11-AS1
2 4 186301446 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs1008728
rs1008728
F11-AS1
2 4 186305519 intron variant C/T snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs10090114
rs10090114
MSRA
1 8 10147444 intron variant T/C snv 0.90 0.700 1.000 1 2019 2019
dbSNP: rs1021230
rs1021230
EBF2
1 8 25928927 intron variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2016 2016
dbSNP: rs10498632
rs10498632
TC2N
2 14 91824400 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10504130
rs10504130
PCMTD1
1 8 51844533 intron variant G/A snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs10747514
rs10747514
PROCR ; MMP24-AS1-EDEM2
1 20 35187566 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10919507
rs10919507 		1 1 170885468 intron variant C/T snv 3.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11057270
rs11057270
SBNO1
1 12 123323526 intron variant T/C snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11132387
rs11132387
F11-AS1
1 4 186297569 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11158204
rs11158204
LOC105370522
1 14 58377808 intron variant C/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs113976843
rs113976843
LINC01681
1 1 170254627 intron variant T/C snv 8.6E-03 0.700 1.000 1 2019 2019