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: rs181362
rs181362
UBE2L3
3 22 21577779 intron variant C/T snv 0.31 0.700 1.000 2 2010 2013
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 2 2012 2013
dbSNP: rs2293889
rs2293889
TRPS1
2 8 115586972 intron variant T/C;G snv 2.0E-04; 0.65 0.700 1.000 2 2010 2013
dbSNP: rs264
rs264
LPL
6 0.882 0.080 8 19955669 intron variant G/A snv 0.14 0.700 1.000 2 2012 2013
dbSNP: rs2652834
rs2652834 		2 15 63104668 intron variant A/C;G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs2923084
rs2923084
AMPD3 ; CAND1.11
2 11 10367235 intron variant A/G snv 0.29 0.700 1.000 2 2010 2013
dbSNP: rs2925979
rs2925979
CMIP
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs2972146
rs2972146 		9 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 0.700 1.000 2 2010 2013
dbSNP: rs3136441
rs3136441
F2
2 11 46721697 intron variant T/C snv 0.13 0.700 1.000 2 2010 2013
dbSNP: rs326
rs326
LPL
4 8 19961928 intron variant A/G snv 0.37 0.700 1.000 2 2012 2013
dbSNP: rs386000
rs386000 		2 19 54288907 intergenic variant C/A;G snv 0.700 1.000 2 2010 2013
dbSNP: rs4129767
rs4129767
PGS1
6 17 78407903 intron variant G/A snv 0.46 0.700 1.000 2 2010 2013
dbSNP: rs4148008
rs4148008
ABCA8
2 17 68879153 non coding transcript exon variant C/G snv 0.40 0.700 1.000 2 2010 2013
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 2 2010 2013
dbSNP: rs4660293
rs4660293
PABPC4
5 1 39562508 non coding transcript exon variant A/C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs4731702
rs4731702
LOC105375508
5 0.925 0.120 7 130748625 intergenic variant C/T snv 0.40 0.700 1.000 2 2010 2013
dbSNP: rs4759375
rs4759375
SBNO1
3 12 123311691 intron variant C/T snv 7.8E-02 0.700 1.000 2 2010 2013
dbSNP: rs4765127
rs4765127
RFLNA ; ZNF664 ; ZNF664-RFLNA
3 12 123975620 intron variant G/T snv 0.33 0.700 1.000 2 2010 2013
dbSNP: rs581080
rs581080
TTC39B
3 9 15305380 intron variant G/C snv 0.72 0.700 1.000 2 2010 2013
dbSNP: rs599839
rs599839
PSRC1
27 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 0.700 1.000 2 2012 2013
dbSNP: rs605066
rs605066 		6 6 139508529 intron variant C/T snv 0.53 0.700 1.000 2 2010 2013
dbSNP: rs6065906
rs6065906 		6 20 45925376 downstream gene variant T/A;C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs6450176
rs6450176
ARL15
4 5 54002195 intron variant G/A snv 0.27 0.700 1.000 2 2010 2013
dbSNP: rs7134375
rs7134375
LOC105369688
3 12 20320824 intergenic variant C/A snv 0.39 0.700 1.000 2 2010 2013
dbSNP: rs7134594
rs7134594
MMAB
4 1.000 0.200 12 109562388 intron variant C/G;T snv 0.700 1.000 2 2010 2013