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: rs6733301
rs6733301
EFR3B
4 0.925 0.080 2 25053415 intron variant G/A snv 0.13 0.700 1.000 1 2008 2008
dbSNP: rs678962
rs678962
DNM3
2 1 172220749 intron variant T/G snv 0.24 0.700 1.000 1 2008 2008
dbSNP: rs6854783
rs6854783
HHIP
2 4 144721927 intron variant G/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs7249094
rs7249094
ADAMTS10
2 19 8607115 intron variant G/A snv 0.45 0.700 1.000 1 2008 2008
dbSNP: rs7846385
rs7846385 		3 8 77247943 intergenic variant T/C snv 0.23 0.700 1.000 1 2008 2008
dbSNP: rs8007661
rs8007661
TRIP11
3 14 91993614 intron variant C/T snv 0.52 0.700 1.000 1 2008 2008
dbSNP: rs8099594
rs8099594 		3 1.000 0.040 18 49464790 upstream gene variant A/C;G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs946053
rs946053
COL27A1
3 1.000 9 114287611 intron variant T/G snv 0.63 0.700 1.000 1 2008 2008
dbSNP: rs2282978
rs2282978
CDK6 ; LOC112268009
5 7 92635096 intron variant T/C snv 0.38 0.700 1.000 3 2008 2009
dbSNP: rs10472828
rs10472828 		2 5 32888712 non coding transcript exon variant C/T snv 0.40 0.700 1.000 2 2009 2009
dbSNP: rs11809207
rs11809207
CATSPER4
2 1 26194649 intron variant G/A snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs13437082
rs13437082 		7 1.000 6 31386783 upstream gene variant C/T snv 0.32 0.700 1.000 1 2009 2009
dbSNP: rs139909
rs139909
TNRC6B
2 22 40301577 intron variant C/T snv 0.74 0.700 1.000 1 2009 2009
dbSNP: rs1569019
rs1569019
ADGRD1
2 12 131091646 intron variant C/A;T snv 8.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs1635852
rs1635852
JAZF1
5 0.882 0.160 7 28149792 intron variant T/C snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs3118914
rs3118914
DLEU1 ; DLEU7
2 13 50542765 intron variant G/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs849141
rs849141
JAZF1
6 0.851 0.240 7 28145472 intron variant A/G snv 0.78 0.700 1.000 1 2009 2009
dbSNP: rs910316
rs910316
TMED10
2 14 75159339 intron variant A/C snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs10513137
rs10513137
ZBTB38
2 3 141424588 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs10010325
rs10010325
TET2 ; TET2-AS1
4 1.000 0.040 4 105185196 intron variant C/A;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs1013209
rs1013209 		2 8 24258791 intergenic variant C/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs10152591
rs10152591
DRAIC ; LOC107984788
2 15 69755818 intron variant A/C snv 9.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs10187066
rs10187066
ZNF142
2 2 218650036 intron variant A/G snv 0.45 0.700 1.000 1 2010 2010
dbSNP: rs1046943
rs1046943
ZBTB24 ; MICAL1
3 1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs1047014
rs1047014
ID4
2 6 19841262 3 prime UTR variant T/C snv 0.23 0.700 1.000 1 2010 2010