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: rs17883880
rs17883880
CHUK
4 10 100230590 intron variant T/A snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs35782247
rs35782247
FANCD2
2 3 10048005 missense variant T/G snv 7.0E-03 2.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787
GAS7
5 17 10058819 intron variant T/C snv 4.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs7836284
rs7836284
MSRA
2 8 10075045 intron variant C/T snv 2.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs7012397
rs7012397
MSRA
2 8 10091523 intron variant A/G snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs11224571
rs11224571
PGR
3 11 101047942 intron variant C/A snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10087178
rs10087178
MSRA
2 8 10111284 intron variant T/C snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs7928851
rs7928851
PGR
3 11 101117160 intron variant C/A snv 1.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs11571151
rs11571151
PGR ; PGR-AS1
6 11 101127486 missense variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10107815
rs10107815
MSRA
4 8 10156645 intron variant G/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs7952037
rs7952037 		3 11 102379653 downstream gene variant C/T snv 1.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs7001567
rs7001567
MSRA
4 8 10257027 intron variant C/G snv 3.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs5030339
rs5030339
ICAM1 ; LOC105372272
5 19 10269461 intron variant G/A snv 3.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs5030359
rs5030359
ICAM1
3 19 10277786 intron variant G/A snv 2.1E-03 0.700 1.000 2 2012 2012
dbSNP: rs5030361
rs5030361
ICAM1
4 19 10278833 intron variant C/T snv 6.8E-04 0.700 1.000 1 2012 2012
dbSNP: rs11828157
rs11828157
MMP13
5 11 102947395 intron variant G/A snv 4.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs675504
rs675504 		5 11 102959002 upstream gene variant A/G snv 0.98 0.700 1.000 1 2012 2012
dbSNP: rs3212121
rs3212121
KLC1 ; XRCC3
2 14 103698185 3 prime UTR variant T/C snv 1.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs10271556
rs10271556
NAMPT
4 7 106258428 intron variant C/T snv 5.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs11193085
rs11193085
SORCS1
3 10 106873848 intron variant G/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs13465
rs13465
ILF3
3 19 10692116 3 prime UTR variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs11813704
rs11813704
SORCS1
2 10 107102114 intron variant G/T snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs3218688
rs3218688
ATM
4 11 108268595 missense variant C/T snv 3.2E-05 2.1E-05 0.700 1.000 1 2012 2012
dbSNP: rs585362
rs585362 		4 1 109247173 upstream gene variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10858082
rs10858082
CELSR2
3 1 109256099 intron variant G/A snv 0.48 0.700 1.000 1 2012 2012