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: rs10146997
rs10146997
NRXN3
6 0.827 0.240 14 79478819 intron variant A/G snv 0.25 0.010 1.000 1 2017 2017
dbSNP: rs1042838
rs1042838
PGR
12 0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
147 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 < 0.001 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: rs11110385
rs11110385 		1 1.000 0.040 12 100458927 intergenic variant C/T snv 0.33 0.010 1.000 1 2015 2015
dbSNP: rs11110386
rs11110386 		1 1.000 0.040 12 100462559 intergenic variant T/C snv 0.33 0.010 1.000 1 2015 2015
dbSNP: rs1111875
rs1111875 		10 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 0.010 1.000 1 2017 2017
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: rs11887534
rs11887534
ABCG5 ; ABCG8
29 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 0.800 1.000 17 2007 2018
dbSNP: rs1205128669
rs1205128669
ABCG8
2 0.925 0.040 2 43877848 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2010 2010
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: rs1248677954
rs1248677954
JMJD1C
1 1.000 0.040 10 63214933 missense variant C/T snv 0.010 1.000 1 2019 2019
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: rs1382897404
rs1382897404
ABCB11
4 0.851 0.040 2 169018071 missense variant C/G snv 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs1399961344
rs1399961344
CYP7A1
1 1.000 0.040 8 58492469 missense variant T/C snv 7.0E-06 0.010 1.000 1 2019 2019
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: rs1478060232
rs1478060232
ABCB11
2 0.925 0.040 2 168969407 missense variant T/C snv 0.010 1.000 1 2010 2010
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