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: rs2114039
rs2114039 		2 1.000 0.080 4 54226459 intron variant T/C snv 0.40 0.800 1.000 2 2011 2013
dbSNP: rs1007000
rs1007000
LPAR1
1 9 110900401 intron variant C/T snv 0.16 0.800 1.000 1 2013 2013
dbSNP: rs1034200
rs1034200 		1 13 22654552 intergenic variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs11145951
rs11145951 		1 9 136965812 upstream gene variant T/C snv 0.44 0.800 1.000 1 2013 2013
dbSNP: rs11204213
rs11204213
RBP3
1 10 47351134 missense variant G/A snv 6.8E-03 2.7E-03 0.800 1.000 1 2014 2014
dbSNP: rs11763147
rs11763147 		1 7 65861834 upstream gene variant A/G snv 0.50 0.800 1.000 1 2013 2013
dbSNP: rs12913547
rs12913547
SMAD3
2 15 67175169 intron variant T/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs12940030
rs12940030 		1 17 14657699 intergenic variant T/C snv 0.45 0.800 1.000 1 2013 2013
dbSNP: rs1324183
rs1324183 		2 1.000 0.040 9 13557492 intron variant A/C;T snv 0.800 1.000 1 2013 2013
dbSNP: rs1536482
rs1536482 		3 1.000 0.040 9 134548682 upstream gene variant G/A snv 0.36 0.800 1.000 1 2013 2013
dbSNP: rs1538138
rs1538138
LINC02542 ; LOC107986617
1 6 82084877 intron variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs1564892
rs1564892
GLT8D2
1 12 104051964 intron variant A/G snv 0.35 0.800 1.000 1 2013 2013
dbSNP: rs17036350
rs17036350
MTOR
1 1 11111169 intron variant C/T snv 9.5E-02 9.6E-02 0.800 1.000 1 2011 2011
dbSNP: rs17084051
rs17084051
RPL22P13
1 4 54221414 non coding transcript exon variant C/A snv 0.25 0.800 1.000 1 2013 2013
dbSNP: rs17103186
rs17103186
LINC01389
1 1 47388842 intron variant C/T snv 2.4E-02 0.800 1.000 1 2014 2014
dbSNP: rs1800813
rs1800813
PDGFRA
1 4 54228300 intron variant G/A snv 0.21 0.800 1.000 1 2014 2014
dbSNP: rs2307121
rs2307121
ADAMTS6
1 5 65329685 intron variant C/T snv 0.27 0.800 1.000 1 2013 2013
dbSNP: rs2444240
rs2444240
TRIM29 ; LOC107984399
1 11 120169734 intron variant T/G snv 0.41 0.800 1.000 1 2012 2012
dbSNP: rs2721051
rs2721051 		3 1.000 0.040 13 40536747 intron variant C/T snv 8.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs3931397
rs3931397
NR3C2
2 1.000 0.080 4 148158346 intron variant G/T snv 0.11 0.800 1.000 1 2013 2013
dbSNP: rs4718428
rs4718428
TMEM248
1 7 66956459 3 prime UTR variant T/A;G snv 0.800 1.000 1 2013 2013
dbSNP: rs4894535
rs4894535
FNDC3B
2 1.000 0.040 3 172277815 intron variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs4938174
rs4938174 		2 11 111042516 upstream gene variant G/A snv 0.31 0.800 1.000 1 2013 2013
dbSNP: rs6496932
rs6496932
ADAMTS7P4
1 15 85282336 intron variant C/A snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs7044529
rs7044529
COL5A1
2 1.000 0.040 9 134676205 intron variant C/T snv 0.21 0.800 1.000 1 2013 2013