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: rs10094715
rs10094715 		2 0.925 0.040 8 46473341 intergenic variant A/G snv 9.8E-03 0.700 1.000 1 2007 2007
dbSNP: rs1011770
rs1011770
BAZ2B
2 0.925 0.040 2 159382207 intron variant A/G snv 2.5E-02 0.700 1.000 1 2007 2007
dbSNP: rs10888095
rs10888095
SGCZ
2 0.925 0.040 8 15004905 intron variant C/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs10998022
rs10998022
MYPN
2 0.925 0.040 10 68210229 intron variant C/T snv 0.26 0.700 1.000 1 2007 2007
dbSNP: rs11186149
rs11186149
SH2D4B
2 0.925 0.040 10 80580951 intron variant T/C snv 8.6E-02 0.700 1.000 1 2007 2007
dbSNP: rs12314274
rs12314274 		2 0.925 0.040 12 85855418 intergenic variant T/C snv 0.37 0.700 1.000 1 2007 2007
dbSNP: rs12362105
rs12362105 		2 0.925 0.040 11 76739864 intergenic variant G/A;T snv 0.700 1.000 1 2007 2007
dbSNP: rs135851
rs135851
C22orf34
2 0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 0.700 1.000 1 2007 2007
dbSNP: rs147194762
rs147194762
ABCG8
2 0.925 0.040 2 43873860 missense variant A/C;G snv 8.0E-06; 3.8E-04 0.010 1.000 1 2008 2008
dbSNP: rs1475029
rs1475029
MIR646HG ; LOC729296
2 0.925 0.040 20 60093953 intron variant A/G snv 0.23 0.700 1.000 1 2007 2007
dbSNP: rs16824658
rs16824658
HMCN1
2 0.925 0.040 1 185895380 intron variant A/G snv 7.6E-02 0.700 1.000 1 2007 2007
dbSNP: rs16843641
rs16843641
TANC1
2 0.925 0.040 2 159061866 intron variant T/C snv 1.2E-02 0.700 1.000 1 2007 2007
dbSNP: rs17063627
rs17063627
GNA14
2 0.925 0.040 9 77424742 intron variant A/G snv 7.2E-02 0.700 1.000 1 2007 2007
dbSNP: rs17066440
rs17066440 		2 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 0.700 1.000 1 2007 2007
dbSNP: rs17088392
rs17088392
DACH1
2 0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 0.700 1.000 1 2007 2007
dbSNP: rs17241442
rs17241442
TNC ; DELEC1
2 0.925 0.040 9 115062806 intron variant G/A snv 0.11 0.700 1.000 1 2007 2007
dbSNP: rs2013647
rs2013647
ZNF28
2 0.925 0.040 19 52827416 intron variant C/T snv 0.11 0.700 1.000 1 2007 2007
dbSNP: rs253314
rs253314
MYO10
2 0.925 0.040 5 16871155 intron variant A/C snv 6.9E-02 0.700 1.000 1 2007 2007
dbSNP: rs2865108
rs2865108 		2 0.925 0.040 7 67861752 intergenic variant C/A snv 0.89 0.700 1.000 1 2007 2007
dbSNP: rs41440452
rs41440452 		2 0.925 0.040 9 122717961 intergenic variant G/A snv 7.9E-02 0.700 1.000 1 2007 2007
dbSNP: rs41506144
rs41506144
FRMD4A
2 0.925 0.040 10 13834687 intron variant C/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs6598902
rs6598902
STX12
2 0.925 0.040 1 27779198 intron variant T/C snv 0.18 0.700 1.000 1 2007 2007
dbSNP: rs738785
rs738785
GUSBP11
2 0.925 0.040 22 23680444 intron variant C/T snv 0.49 0.700 1.000 1 2007 2007
dbSNP: rs749661564
rs749661564
ABCG8
2 0.925 0.040 2 43852775 missense variant C/T snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs8061765
rs8061765
TMEM114
2 0.925 0.040 16 8540871 intron variant G/A snv 0.11 0.700 1.000 1 2007 2007