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: rs10025152
rs10025152
F11-AS1
2 4 186304150 intron variant G/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs10029715
rs10029715
F11-AS1
2 4 186301446 intron variant T/C snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs1008728
rs1008728
F11-AS1
2 4 186305519 intron variant C/T snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1018827
rs1018827
F5
2 1 169544768 intron variant A/G snv 0.92 0.700 1.000 1 2012 2012
dbSNP: rs11132388
rs11132388
F11-AS1
1 4 186298264 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs112477227
rs112477227
F11-AS1
1 4 186310896 intron variant C/A snv 9.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs114101204
rs114101204
LINC00970
1 1 169056816 intron variant G/A snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs114964168
rs114964168
LINC00970
1 1 169063639 intron variant C/T snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs117784795
rs117784795
PTPRJ
2 11 48030514 intron variant C/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs1200063
rs1200063
NME7
1 1 169345192 intron variant T/C snv 0.95 0.700 1.000 1 2012 2012
dbSNP: rs1208134
rs1208134
CCDC181
2 1 169459706 intron variant C/T snv 0.93 0.700 1.000 1 2012 2012
dbSNP: rs1208135
rs1208135
CCDC181
2 1 169454860 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1208327
rs1208327
NME7
2 1 169327626 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1209731
rs1209731
NME7
2 1 169355555 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs12500826
rs12500826
F11-AS1
2 4 186306297 intron variant T/C snv 0.60 0.700 1.000 1 2012 2012
dbSNP: rs138315285
rs138315285
PTPRJ
1 11 48042642 intron variant G/A snv 9.9E-03 0.700 1.000 1 2012 2012
dbSNP: rs140541052
rs140541052
SPI1
1 11 47368220 intron variant C/G snv 1.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs144737447
rs144737447
NME7
1 1 169191220 intron variant C/T snv 1.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs144915398
rs144915398
NDUFS3 ; KBTBD4
2 11 47576929 intron variant G/A snv 1.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs150341456
rs150341456
FNBP4
2 11 47762062 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1633513
rs1633513
ABO
1 9 133265051 intron variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs16861990
rs16861990
NME7
2 1 169165889 intron variant A/C snv 5.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs17474001
rs17474001
STKLD1
1 9 133402020 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs1752339
rs1752339
ABO
1 9 133265724 intron variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs2036914
rs2036914
F11
5 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012