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: rs202148845
rs202148845 		1 1 173081132 intergenic variant -/A delins 0.700 1.000 1 2013 2013
dbSNP: rs57476984
rs57476984
LIPC ; ALDH1A2
1 15 58426498 intron variant -/A delins 1.4E-05 0.700 1.000 1 2012 2012
dbSNP: rs113226428
rs113226428
FAM155A ; FAM155A-IT1 ; LOC107984581
1 13 107817853 intron variant -/C ins 0.700 1.000 1 2012 2012
dbSNP: rs57277452
rs57277452
LOC102723763
1 4 2772731 intergenic variant -/C ins 8.1E-04 0.700 1.000 1 2012 2012
dbSNP: rs61435922
rs61435922
LINC01499
1 11 41756060 intron variant -/C ins 0.13 0.700 1.000 1 2012 2012
dbSNP: rs34910943
rs34910943 		1 11 61653517 downstream gene variant -/CTCTG ins 0.700 1.000 1 2012 2012
dbSNP: rs200666086
rs200666086
PYROXD2
1 10 98397611 intron variant -/CTG delins 0.700 1.000 1 2013 2013
dbSNP: rs11437675
rs11437675
VPS37C
1 11 61150558 intron variant -/G ins 3.2E-03 0.700 1.000 1 2012 2012
dbSNP: rs34766626
rs34766626
VPS37C
1 11 61144420 non coding transcript exon variant -/G delins 0.700 1.000 1 2012 2012
dbSNP: rs35088638
rs35088638
CETP
1 16 56962246 5 prime UTR variant -/G delins 0.700 1.000 1 2012 2012
dbSNP: rs35713313
rs35713313
CLTCL1
1 22 19275329 intron variant -/G delins 0.700 1.000 1 2012 2012
dbSNP: rs4019045
rs4019045
ERBIN
1 5 65982680 intron variant -/GACTG ins 0.82 0.700 1.000 1 2012 2012
dbSNP: rs35328399
rs35328399
KLKB1
1 4 186217309 intron variant -/GTT delins 0.700 1.000 1 2012 2012
dbSNP: rs146534688
rs146534688 		1 4 64155298 intergenic variant -/TA;TATACATA delins 0.700 1.000 1 2012 2012
dbSNP: rs201608675
rs201608675 		1 11 61653518 downstream gene variant -/TCTCTGG;TCTGG ins 0.83 0.700 1.000 1 2012 2012
dbSNP: rs33930717
rs33930717
KLKB1
1 4 186257634 intron variant -/TGT;TTT delins 0.700 1.000 1 2012 2012
dbSNP: rs35826599
rs35826599
CLTCL1
1 22 19269948 intron variant A/-;AA delins 0.700 1.000 1 2012 2012
dbSNP: rs35253168
rs35253168
SLC16A10
1 6 111199828 intron variant A/-;AA;AAA;AAAA;AAAAA delins 0.700 1.000 1 2012 2012
dbSNP: rs386408250
rs386408250
SLC16A10
1 6 111199828 intron variant A/-;AA;AAA;AAAA;AAAAA delins 0.22 0.700 1.000 1 2012 2012
dbSNP: rs174536
rs174536
MYRF ; TMEM258
3 11 61784455 non coding transcript exon variant A/C snv 0.29 0.700 1.000 2 2012 2013
dbSNP: rs10141869
rs10141869
LOC105370504
1 14 53665936 intron variant A/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs1037920
rs1037920
ARNTL2 ; ARNTL2-AS1
1 12 27400808 intron variant A/C snv 0.19 0.13 0.700 1.000 1 2013 2013
dbSNP: rs1052335
rs1052335
TPD52L3
1 9 6330380 3 prime UTR variant A/C snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs1061388
rs1061388
REV3L ; MFSD4B
1 6 111299091 3 prime UTR variant A/C snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs10741271
rs10741271 		1 10 127467534 intergenic variant A/C snv 0.79 0.700 1.000 1 2013 2013