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: rs34729281
rs34729281
SUGP2
2 19 19009572 intron variant -/G delins 0.700 1.000 1 2012 2012
dbSNP: rs11216126
rs11216126 		4 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs353616
rs353616
CD44
2 11 35155029 intron variant A/C snv 1.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs3858076
rs3858076
ABCA1
3 9 104893841 intron variant A/C snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs480392
rs480392
NTNG1
3 1 107436774 synonymous variant A/C snv 0.99 0.95 0.700 1.000 1 2012 2012
dbSNP: rs643830
rs643830
NCAM1
2 11 113235826 intron variant A/C snv 1.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs6726798
rs6726798
VIL1
3 2 218436132 intron variant A/C snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs6810819
rs6810819
NOCT
2 4 139015171 upstream gene variant A/C snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs7000460
rs7000460
LPL
3 8 19946291 intron variant A/C snv 7.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs7203984
rs7203984
CETP
7 16 56965346 intron variant A/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs7222232
rs7222232
GAS7
2 17 10033485 intron variant A/C snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs4660293
rs4660293
PABPC4
5 1 39562508 non coding transcript exon variant A/C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs10489615
rs10489615
GALNT2
3 1 230169242 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs2075847
rs2075847
MMP1 ; WTAPP1
3 11 102799093 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2863973
rs2863973
SMPD3
2 16 68375532 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		15 0.763 0.200 2 226203364 intergenic variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs4784745
rs4784745
CETP
2 16 56980963 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2652834
rs2652834 		2 15 63104668 intron variant A/C;G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs2980875
rs2980875 		6 8 125469505 intron variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12394306
rs12394306
SYN1
4 X 47576648 splice region variant A/C;T snv 4.3E-03 0.700 1.000 1 2012 2012
dbSNP: rs289715
rs289715
CETP
2 16 56974596 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4245232
rs4245232
LIPG
2 18 49560628 upstream gene variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs485671
rs485671
LIPC ; ALDH1A2 ; LIPC-AS1
5 15 58448935 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs486394
rs486394
LINC02702
4 1.000 0.040 11 116655605 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4986970
rs4986970
LCAT
4 0.925 0.080 16 67942417 missense variant A/C;T snv 4.0E-06; 1.7E-02 0.700 1.000 1 2012 2012